Skip to main content

Respiratory syncytial virus prophylaxis for prevention of recurrent childhood wheeze and asthma: a systematic review



Acute bronchiolitis caused by respiratory syncytial virus (RSV) has been associated with greater risk of recurrent wheezing and asthma. However, it is unclear whether this association is causal. RSV-specific monoclonal antibodies have been shown to reduce RSV-related hospitalisations in high-risk infants, but the longer-term follow-up has given conflicting evidence for prevention of recurrent wheeze or asthma.


We performed a systematic review and meta-analysis to determine whether monoclonal antibody prophylaxis against RSV bronchiolitis reduces the risk of subsequent recurrent wheeze or asthma. If so, this may support the hypothesis of causality.


Studies were identified via an online database search using Embase, MEDLINE, PubMed, Web of Science and the Cochrane Library. Manufacturers of monoclonal antibodies were contacted directly for unpublished data. The intervention of interest was RSV monoclonal antibody prophylaxis, and the primary outcome measure was recurrent wheeze and/or asthma. Studies were screened according to inclusion/exclusion criteria. Included studies were evaluated for quality and assessed for bias independently by 3 reviewers using the ‘Grading of Recommendations Assessment, Development and Evaluation’ (GRADE) approach. Results were extracted into 2 × 2 outcome tables and a meta-analysis carried out producing forest plots based on relative risk. Heterogeneity was assessed using the I2 statistic.


The search identified 141 articles, which, after screening, resulted in eight studies (2 randomised controlled trials), thus including 11,195 infants in the meta-analysis. The overall result demonstrated a non-statistically significant reduction in relative risk of developing recurrent wheeze or asthma (RR 0.60; 95% CI 0.31 to 1.16). Study quality was generally low with evidence of publication bias and statistical heterogeneity. However, sub-group analysis excluding studies deemed to be ‘very low’ quality showed a relative risk of 0.42 (95% CI 0.22 to 0.80, p = 0.008). A further sub-group analysis for infants aged 32 to < 36 weeks showed a statistically significant relative risk of 0.35 (95% CI 0.14 to 0.86, p = 0.02).


We did not identify an overall statistically significant benefit. However, our two sub-group analyses did find statistically significant benefits of monoclonal antibody therapy on the risk of recurrent wheeze and asthma. The main limitation of this study is the lack of high-quality randomised controlled trials, highlighting the need for more research in this field.

Peer Review reports


Bronchiolitis, an acute lower respiratory tract infection (LRTI), is the most common reason for hospitalisation in young children in many countries including the UK and USA [1]. The majority of young children will experience bronchiolitis, with approximately 3% requiring hospital admission [1]. LRTIs in early life, particularly in infancy, are associated with development of recurrent wheeze and asthma in later childhood [2]. Pre-term infants especially are at an increased risk of both severe bronchiolitis and recurrent wheeze or asthma development independently [3, 4].

Recurrent wheeze in infancy is common, with one large international study of infants reporting that 45% had at least one wheezing episode, and 20% had three or more [5]. This can have a substantial effect on health-related quality of life for infants and their families [6]. When recurrent attacks of wheezing continue to occur as the child ages, an asthma diagnosis becomes more likely. Asthma is the most prevalent chronic respiratory disease worldwide, and its pathogenesis is multifactorial with hypersensitivity and inflammation of the airways leading to wheeze and shortness of breath [7, 8]. It has been estimated that the cost of asthma is approximately £1.1 billion in the UK, highlighting it as a key public health issue [9]. It creates a huge burden on both patients and health services in terms of health-related quality of life and cost, with the most significant impact being amongst lower socioeconomic groups and ethnic minorities [10]. With the overall prevalence increasing globally, further research is needed into why this increase is happening, and whether or not there any preventative measures that can be undertaken [10].

Acute bronchiolitis in early life is very strongly associated with an increased risk of asthma development [11]. It has been shown that infants hospitalised with acute bronchiolitis have a significantly increased risk of developing childhood wheeze and asthma, with one study from Finland finding the risk of recurrent wheeze or asthma development post hospitalised bronchiolitis to be twice that of the general population [12]. However, while this association is well established, debate remains over whether acute bronchiolitis is merely the first manifestation of recurrent wheeze or asthma or contributes to causation. To assess causality, studies assessing the impact of bronchiolitis prevention on the outcome of subsequent development of recurrent wheeze and asthma are needed [11].

The most common cause of acute bronchiolitis is respiratory syncytial virus (RSV), primarily occurring in infants up to 12 months. RSV-specific monoclonal antibodies provide passive immunity and have shown efficacy in reducing RSV hospitalisations in high-risk infants, such as those born prematurely [13,14,15]. Currently, immunoprophylaxis is only deemed cost-effective in very early pre-term infants (< 32 weeks’ gestational age) for prevention of severe RSV bronchiolitis. Palivizumab is the most common RSV-specific monoclonal antibody in use and has been shown to be well tolerated with very low rates of minor adverse events such as injection site reaction, fever, diarrhoea, and irritability [16]. Motavizumab, a palivizumab derivative, is a second-generation humanised monoclonal antibody. Initially hoped to have greater efficacy and lower dose requirement when compared to palivizumab [16, 17], motavizumab was discontinued in 2010 due side effect concerns, particularly in regard to serious skin reactions, and doubts over superior efficacy to palivizumab [16, 18, 19]. Other palivizumab biosimilars have been developed including nirsevimab, which has a longer half-life than palivizumab [20]. Lunamab is another RSV-specific monoclonal antibody developed as a less-expensive biosimilar aimed at low-income countries [21]. Another biosimilar antibody, suptavumab, was withdrawn in 2017 due to failure to meet primary endpoint in clinical trial testing [22].

Monoclonal antibodies are prohibitively expensive and the estimated cost of palivizumab is approximately £3000–£5000 ($3700–$6200 USD) per child [23]. Despite proven efficacy and the high prevalence of RSV infection in infancy, most children will not experience a severe RSV-related illness and thus delivery of monoclonal antibody therapy to all infants is not currently considered cost-effective [23, 24]. Smart et al. in their systematic review of the cost-effectiveness of RSV prophylaxis on the outcome of RSV bronchiolitis found it to be cost-effective for high-risk groups including very early pre-term infants (< 32 weeks), children with congenital heart disease and those of Aboriginal descent [25]. They also noted for infants born at 33–35 weeks gestational age, RSV prophylaxis could be considered cost-effective in the presence of additional risk factors including chronological age, number of siblings, history of atopy, absence of breast feeding, cigarette smoke exposure and daycare attendance [26].

To further examine the relationship between RSV bronchiolitis and subsequent development of recurrent wheeze and asthma, we conducted a systematic review and meta-analysis to determine whether monoclonal antibody RSV prophylaxis compared with no prophylaxis, in infants born from early pre-term up to term, reduces the risk of recurrent wheeze or asthma development in later childhood.


Protocol and registration

The review protocol is registered with PROSPERO (CRD42019i28239) and is accessible at Findings are reported according to the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) standards (Additional file 1).

Inclusion criteria

Types of studies and participants

Table 1 summarises the inclusion/exclusion criteria used in study screening. Primary studies including randomised control trials (RCTs), prospective observational case-control studies and cohort studies were included. We only included studies enrolling pre-term infants (up to full term), who were subsequently followed up until infancy or childhood (1–10 years).

Table 1 Inclusion and exclusion criteria used when screening articles first by title and abstract and then by full text. Papers were included if they were primary studies of any study design. The population being studied was infants born early pre-term up to term. The studies were investigating monoclonal antibody prophylaxis compared with no prophylaxis or placebo, on the outcome of recurrent wheeze or asthma. No studies investigating a population of infants with congenital defects were included, and no other RSV prophylaxis or treatment apart from monoclonal antibody was considered

Intervention, comparison and outcome

The intervention being investigated was the use of RSV-specific monoclonal antibodies for RSV immunoprophylaxis compared to no RSV prophylaxis or placebo. The only outcome measured was development of subsequent recurrent wheeze and/or asthma as defined by the study authors, including parent-reported wheeze as well as formally doctor-diagnosed wheeze or asthma. Parent-reported wheeze is an important outcome to include as not all infants who wheeze will be assessed by a physician. Other outcomes such as RSV hospitalisation or allergy diagnosis were assessed in some studies; however, these are not a priority for this review.

Information sources and search strategy

The literature search, using the strategy in Table 2, was conducted using Embase, MEDLINE, PubMed, Web of Science and the Cochrane Library. We also contacted the manufacturers of RSV-specific monoclonal antibodies for any unpublished data, and searched trial registries such as ‘’ and ‘BMC Trials’ and the WHO International Clinical Trials Registry, for any potentially suitable studies that may be imminently reported and published. The date last searched was July 2020. Reference lists of included and other relevant papers were hand searched to identify possible additional primary studies.

Table 2 Search strategy. An example of the comprehensive literature search performed across the electronic databases, with search terms and limitations applied. Shown search strategy example is from MEDLINE

Data collection and analysis

Selection of studies

Studies were independently screened according to inclusion and exclusion criteria by 2 independent reviewers (HG and MS). The screening was a 2-step process, first by title and abstract, and then by full text. A third-party reviewer was involved in the case of any disagreements. Duplicate articles, identified using reference software, were removed.

Data extraction and management

Data were extracted using an adapted form of the ‘Data collection form for Intervention review—RCTs and non-RCTs’ of the Cochrane Collaboration [27] (Additional file 2). Data is presented in the summary of findings table which includes study type, population number, number in intervention and comparison groups, 2 × 2 outcome tables, relative risk and evaluation of the quality of evidence and bias risk as per Cochrane handbook guidance [28].

Risk of bias

Study validity was evaluated using the Cochrane Risk of Bias table, and overall quality of evidence was evaluated independently by 3 reviewers using the ‘Grading of Recommendations Assessment, Development and Evaluation’ (GRADE) approach as detailed in our protocol [29].

Data synthesis and meta-analysis

Using the main outcome of recurrent wheeze (dichotomous—yes/no) and the data from the 2 × 2 outcome tables produced, a meta-analysis was performed using a random effects model, with relative risk as the principal summary measure. Individual studies are represented on a forest plot based on relative risk and 95% confidence intervals. Funnel plots were generated to portray publication bias or possible selective reporting within studies. StatsDirect statistical software was used for the meta-analysis [30].


To test for heterogeneity (inconsistency between studies), we used the I2 test, taking an I2 of > 75% as being high heterogeneity.

Sub-group analysis

Sub-group analysis of late pre-term infants was performed to explore the effectiveness of RSV prophylaxis on subsequent recurrent wheeze in this population. Sub-group analysis excluding very low-quality evidence was also carried out, due to the risk of confounding by indication.


The search across the main databases generated 141 references. After removal of duplicate papers and full-text screening, eight studies were included in this review (Fig. 1). These included two RCTs, four cohort studies, one case-control study and one cross-sectional study. Reasons for the studies excluded after full-text review are outlined in Additional file 2. Study characteristics for which data was extracted are presented in the summary of findings table (Table 3).

Fig. 1

PRISMA flow diagram. Study screening and selection outlined using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flow diagram [31]. This process resulted in 8 studies being included in the final quantitative meta-analysis

Table 3 Summary of findings table. Study characteristics for which data was extracted for each study are presented in this table. These include number of participants, length of follow-up, outcomes, relative risk and the GRADE assessment for quality of evidence and bias risk

In total, 11,195 infants were included in this review. The gestational age of participants ranged from 24 weeks to full term and the median length of follow-up across the studies was 4 years (range 2 to 6 years). Of the 8 studies, 5 reported a reduction in recurrent wheeze after RSV-specific monoclonal antibody prophylaxis.

Quality of evidence was variable. The two RCTs were considered as high-quality evidence, with most other studies graded as low-quality evidence. The funnel plot in Fig. 2 is likely to reflect publication bias, but could also represent selective reporting within studies, or poor methodology, which is in keeping with the GRADE assessment of bias outlined in Table 3. We noted a significant number of manufacturer-funded studies creating the potential for sponsorship bias. There was considerable statistical heterogeneity between studies (I2 96.6%; 95% confidence interval [CI] 95.4 to 97.3%).

Fig. 2

Publication bias. Funnel plot highlighting the risk of publication bias in results. More precise results are plotted near the top (lower standard error). Points plotted outside the funnel indicate high risk of publication bias

Figure 3 displays the forest plot of pooled relative risks, derived using a random effects model to allow for heterogeneity. Overall, RSV monoclonal antibody prophylaxis did not confer a statistically significant benefit on the reduction of the risk of recurrent wheeze or asthma (relative risk [RR] 0.60; 95% CI 0.31 to 1.16, p = 0.129).

Fig. 3

Overall result of meta-analysis. Using a random effects model, a meta-analysis was performed and a forest plot constructed using relative risk as the summary measure. This shows a pooled relative risk for the primary outcome of 0.60 with use of monoclonal antibody prophylaxis; however, results are not statistically significant

Sub-group analyses

Two studies (Carroll et al. and Simoes et al.) [35, 38] were graded as being of very low quality with serious risk of bias. Carrol et al.’s study was deemed to show considerable risk of bias given infants most at risk of both RSV and development of recurrent wheeze were more likely to have increased uptake and compliance with monoclonal antibody prophylaxis, potentially skewing results. In the report by Simoes et al., there was a serious risk of confounding due to the fact that the average gestational age of the palivizumab-treated group was 28 weeks, compared with 34 weeks in the untreated group such that infants in the treated group were already at an increased risk of RSV and recurrent wheeze. In view of the significant confounding for these two studies, a sub-group analysis excluding these studies was performed (Fig. 4). This resulted in a significant reduction in relative risk of 0.42 (95% CI 0.22 to 0.80) for the primary outcome (p = 0.008).

Fig. 4

Meta-analysis with very low-quality studies removed. Two studies carried a significant risk of bias by confounding, skewing the results and showing the opposite effect to the overall result. Upon removal of these studies in a sub-group analysis, the overall pooled relative risk became statistically significant at 0.42 (95% CI = 0.22 to 0.80)

To investigate the moderate to late pre-term cohort, a pre-specified sub-group analysis was planned for infants whose gestational age was 33–35 weeks. However, only 3 papers specifically focused on this later pre-term cohort. To allow for this sub-group meta-analysis to be performed using available study data, we adjusted the gestational age range included to be 32 to < 36 weeks. In this sub-group, we found that infants who received monoclonal antibody prophylaxis had a significant reduction in relative risk of developing wheeze or asthma (RR 0.35; 95% CI 0.14 to 0.86, p = 0.02) (Fig. 5).

Fig. 5

Sub-group analysis among pre-term infants with gestational age 32 to < 36 weeks. This sub-group analysis demonstrates a relative risk of 0.35 (95% CI = 0.14–0.86), showing a statistically significant reduction in risk of recurrent wheeze among this cohort of preterm infants with palivizumab use

Safety and adverse effects

Safety data regarding monoclonal antibody use were not reported for most studies, with the exception of one RCT, comparing motavizumab with placebo in 1919 infants, reported by O’Brien et al. In this study, eight serious adverse events were associated with use of motavizumab, all within one day of dosing. Six were consistent with hypersensitivity type reactions, one appeared as erythema multiforme and one was self-resolving skin erythema [33].


This systematic review aimed to evaluate evidence around whether RSV prophylaxis, using monoclonal antibodies, reduced the risk of pre-term infants developing recurrent wheeze or asthma in childhood. According to our primary analysis, including all studies regardless of quality, and infants of all gestational ages, we did not identify a statistically significant benefit for this outcome. However, our two pre-defined sub-group analyses, in which we excluded studies of very low quality, and separately focussed on infants born after 32 weeks gestation, did find statistically significant benefits on monoclonal antibody therapy on the risk of recurrent wheeze and asthma.

We noted three studies whose relative risk results showed a different effect to the overall result. O’Brien et al. showed a relative risk of 1.10 for the primary outcome with monoclonal antibody prophylaxis using motavizumab [33]. They concluded that prophylaxis with motavizumab had no effect on subsequent recurrent wheeze. However, the reported confidence intervals are extremely wide, meaning that the true effect could lie anywhere between 0.61 and 1.97. When assessing quality of this evidence using the GRADE approach, it was concluded as being a high-quality study. It was a RCT with a low risk of recall or sponsorship bias. However, it is important to note it was performed in a population of Native American infants only, who have been shown to be at an increased risk of serious RSV bronchiolitis, with the RSV-associated hospital admission rate being almost 2.5 times that of infants in the general US population of the same age [40, 41]. Another important factor to consider is that this study was the only study investigating motavizumab as the monoclonal antibody prophylaxis. While motavizumab has been proven to be efficacious in terms of reducing RSV hospitalisations in various studies, this study was the first to assess its efficacy in reducing recurrent wheeze [18, 33]. Thus, results for this study may not be as generalizable to use of other monoclonal antibodies in a non-native American population.

Carroll et al. report a cohort study which also appeared to show the opposite effect to the overall pooled effect [35]. When using the GRADE approach to assess the quality of each study, this study was found to have a considerable risk of confounding. The authors report measuring adherence to palivizumab as 0% adherence, < 70% adherence and > 70% adherence; however, due to the specificities of the research question in our systematic review, the < 70% adherence group and the > 70% adherence group were combined. Accordingly, many included patients in the treatment group may not have received the intervention. Furthermore, more infants in the > 70% adherence group had chronic lung disease, lower median birth weight and longer median birth hospital stay and also were generally smaller for gestational age than in the other groups [35]. These are all known risk factors for increased severity of RSV infection and subsequent childhood wheeze [42,43,44,45]. Accordingly, this may have skewed results and may account for the observation in this study that palivizumab use was significantly associated with increased risk of recurrent wheeze [35].

The cross-sectional study carried out by Simoes et al. in 2019 also demonstrated a seemingly opposite result to the overall pooled result [38]. When assessing quality of evidence, this paper was also deemed to be very low quality due to confounding in relation to gestational age. There was a significant difference in mean gestational age between the palivizumab-treated group and the untreated group, 28 weeks and 34 weeks respectively. As a result, this study also appears to show that palivizumab use is associated with an increased risk of recurrent wheeze [38].

The remaining studies each showed a significant reduction in relative risk for the primary outcome with use of monoclonal antibody prophylaxis. However, it is important to highlight that the quality of this evidence varied widely and was mostly graded as low-quality evidence, with only one high-quality RCT—the MAKI Trial [36].

Recurrent wheeze represents a huge public and global health problem. It has been estimated that the cost of asthma is approximately £1.1 billion in the UK [9]. On the level of the individual child affected, recurrent childhood wheeze can significantly impact quality of life. It can lead to inability to partake in physical exercise and play and, thus, affect the child’s education and development [46]. There is also substantial burden on the family in terms of working days lost for parents/carers. A recent epidemiological study using electronic health care records to estimate the prevalence of recurrent wheeze found that parent-reported wheezing prevalence was 12.9% [47]. Thus, any intervention to reduce recurrent wheeze prevalence would have the potential to significantly improve the lives of many children and families as well as having considerable financial benefits.

Monoclonal antibodies are expensive, and analyses based on RSV bronchiolitis outcomes suggest their use is only cost-effective for certain high-risk groups, such as early pre-term infants (< 32 weeks). However, later pre-term infants aged between 32 and 36 weeks gestation also have high RSV hospitalisation rates (3.75% and 9.8%) and immunological differences in lung development [48]. Our pre-specified sub-group analysis of 3 studies focusing on infants with gestational age ranging from 32 weeks to 36 weeks showed a statistically significant relative risk of 0.35, suggesting that some infants in this cohort may benefit from RSV prophylaxis to reduce their risk of subsequent recurrent wheeze. Cost-effectiveness analysis of RSV prophylaxis, based on the composite outcome of RSV bronchiolitis and recurrent wheeze in this specific gestational category, is necessary to draw more robust conclusions about this issue.

While there is an established association between RSV infection and subsequent recurrent wheeze, there is question of whether or not this recurrent wheeze can be called asthma. The MAKI trial (Scheltema et al.) was initially published in 2013 as a 1-year follow-up study; however, in this systematic review, we included the 6-year follow-up data. The original 1-year study found a statistically significant reduction in the proportion of infants with recurrent wheeze in the palivizumab-treated group [49]. In the 6-year follow-up study, while a significant difference between treatment and control groups in parent-reported asthma at age 6 years was noted, no significant difference in lung function tests or physician diagnosed asthma was evident [36]. Prais et al. reported in 2016 the results of a study on the short- and long-term effects of palivizumab use in premature infants and reported a significant reduction in rates of recurrent wheeze during the first 2 years of life in those who received palivizumab (27% compared to 70% in the untreated group) [50]. However, by school age (7–10 years), there was no significant difference in recurrent wheeze or pulmonary function tests. This suggests that monoclonal antibody prophylaxis may have a protective effect on the airway short term but not long term. Data from this study were not included in this meta-analysis due to the fact that the majority of infants included were diagnosed with bronchopulmonary dysplasia [50].

RSV infection itself causes direct damage to the lungs, particularly in premature infants, for example ciliary destruction, necrosis of epithelial cells, inflammation of the submucosa and bronchiolar plugging from mucous secretions [50]. Considering this and the fact that studies have shown no significant effect of RSV prophylaxis on lung function at school age, it could be hypothesised that post-RSV recurrent wheeze may not represent atopic asthma but rather results from direct damage of the RSV infection to the lungs which gradually improves with time and age. This is supported by previous work by Martinez et al. who investigated factors affecting wheezing before the age of 3 years and at 6 years and concluded most infants who wheeze do not have an increased risk of asthma or allergy later in life [51]. Using the same study population as Simoes et al. [32], the same research team explored the protective effect of palivizumab prophylaxis on recurrent wheeze in atopic vs non-atopic children. They found that immunoprophylaxis reduced the relative risk by 80% in non-atopic children, but had no effect in those with a family history of atopy [52]. Taking all this into consideration, it may be that RSV prophylaxis with monoclonal antibody reduces the risk of RSV infection in certain groups by preventing the airway from direct damage by RSV and reducing subsequent risk of recurrent wheeze. However, if the mechanism by which RSV causes recurrent wheeze is independent of atopy, in children with an atopic predisposition, RSV prophylaxis would not reduce the risk of subsequent or asthma.

Study limitations

Firm conclusions from this systematic review are hindered by the lack of good-quality evidence. Only eight studies were eligible to be included in the review and of these 8, only 2 were considered to be of high quality. The significant statistical heterogeneity between the studies and publication bias found is likely to affect the overall pooled results of this meta-analysis, introducing significant risk of bias. Ideally, more RCTs are needed to investigate the role of monoclonal antibody prophylaxis on the outcome of recurrent wheeze. However, such RCTs in at-risk populations would be difficult given the proven benefit of palivizumab in prevention of severe RSV bronchiolitis in pre-term infants. A further major limitation is the lack of long-term follow-up in the studies included. This meant that our outcome used was recurrent wheezing rather than true asthma. Further studies with longer follow-up are required to address the question of RSV prevention and asthma causation.

The main strength of this systematic review and meta-analysis is the thorough literature search, careful study selection with strict inclusion criteria, and comprehensive assessment of bias using the established GRADE approach. Furthermore, the findings of this study are in support of existing evidence for the association between RSV bronchiolitis and recurrent wheeze/asthma.


It is still unclear whether administering RSV prophylaxis to pre-term infants reduces the risk of respiratory complications later in childhood. On the basis of pre-specified sub-group analyses excluding low-quality studies, and focusing on late pre-term infants, we conclude that potential long-term benefits cannot be ruled out. This review highlights the need for longer-term high-quality clinical trials investigating RSV prophylaxis on the outcome of asthma, as current evidence is of very limited quality. In particular, there should be a focus on these benefits in late pre-term infants (32–36 weeks).

Availability of data and materials

All data was obtained from studies included in reference list [32,33,34,35,36,37,38,39]



Grading of Recommendations Assessment, Development and Evaluation


Respiratory syncytial virus


  1. 1.

    Øymar K, Skjerven HO, Mikalsen IB. Acute bronchiolitis in infants, a review. Scand J Trauma Resusc Emerg Med. 2014;22:23 Published 2014 Apr 3.

    Article  Google Scholar 

  2. 2.

    van Meel ER, den Dekker HT, Elbert NJ, Jansen PW, Moll HA, Reiss IK, de Jongste JC, Jaddoe VWV, Duijts L. A population-based prospective cohort study examining the influence of early-life respiratory tract infections on school-age lung function and asthma. Thorax. 2018;73(2):167–173.

  3. 3.

    Stranak Z, Saliba E, Kosma P, Posfay-Barbe K, Yunis K, Farstad T, et al. Predictors of RSV LRTI hospitalization in infants born at 33 to 35 weeks gestational age: a large multinational study (PONI). PLoS One. 2016;11(6):e0157446.

    Article  Google Scholar 

  4. 4.

    Sonnenschein-van der Voort AMM, Arends LR, de Jongste JC, Annesi-Maesano I, Arshad SH, Barros H, et al. Preterm birth, infant weight gain, and childhood asthma risk: a meta-analysis of 147,000 European children. J Allergy Clin Immunol. 2014;133(5):1317–29.

    Article  Google Scholar 

  5. 5.

    Mallol J, Garcia-Marcos L, Sole D, Brand P. International prevalence of recurrent wheezing during the first year of life: variability, treatment patterns and use of health resources. Thorax. 2010;65(11):1004–1009.

  6. 6.

    Oostenbrink R, Jansingh-Piepers EM, Raat H, Nuijsink M, Landgraf JM, Essink-Bot ML, et al. Health-related quality of life of pre-school children with wheezing illness. Pediatr Pulmonol. 2006;41(10):993–1000.

    CAS  Article  Google Scholar 

  7. 7.

    Krishnan JA, Lemanske RF, Canino GJ, Elward KS, Kattan M, Matsui EC, et al. Asthma outcomes: asthma symptoms. J Allergy Clin Immunol. 2012;129(30):1004–1009.

  8. 8.

    Soriano JB, Abajobir AA, Abate KH, Abera SF, Agrawal A, Ahmed MB, et al. Global, regional, and national deaths, prevalence, disability-adjusted life years, and years lived with disability for chronic obstructive pulmonary disease and asthma, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015. Lancet Respir Med. 2017;5(9):691–706.

  9. 9.

    Mukherjee M, Stoddart A, Gupta RP, Nwaru BI, Farr A, Heaven M, et al. The epidemiology, healthcare and societal burden and costs of asthma in the UK and its member nations: analyses of standalone and linked national databases. BMC Med. 2016;14(1):113. Available from:

  10. 10.

    Loftus PA, Wise SK. Epidemiology of asthma. Curr Opin Otolaryngol Head Neck Surg. 2016;24(3):245–249.

  11. 11.

    Feldman AS, He Y, Moore ML, Hershenson MB, Hartert TV. Toward primary prevention of asthma. Reviewing the evidence for early-life respiratory viral infections as modifiable risk factors to prevent childhood asthma. Am J Respir Crit Care Med. 2015;191(1):34–44.

    Article  Google Scholar 

  12. 12.

    Törmänen S, Lauhkonen E, Riikonen R, Koponen P, Huhtala H, Helminen M, et al. Risk factors for asthma after infant bronchiolitis. Allergy. 2018;73(4):916–22.

  13. 13.

    Utrecht University. First consortium of local manufacturers to make affordable biosimilars available for low income countries.

  14. 14.

    Olchanski N, Hansen RN, Pope E, D’Cruz B, Fergie J, Goldstein M, et al. Palivizumab prophylaxis for respiratory syncytial virus: examining the evidence around value. Open forum Infect Dis. 2018;5(3):ofy031.

    Article  Google Scholar 

  15. 15.

    Rogovik AL, Carleton B, Solimano A, Goldman RD. Palivizumab for the prevention of respiratory syncytial virus infection. Can Fam Physician. 2010;56(8):769–72.

  16. 16.

    Bernhard R. Product review on the monoclonal antibody palivizumab for prevention of respiratory syncytial virus infection. Hum Vaccin Immunotherapeutics. 2017;13(9):2138–49.

    Article  Google Scholar 

  17. 17.

    Cingoz O. Motavizumab. MAbs. 2009;1(5):439–42.

    Article  Google Scholar 

  18. 18.

    Carbonell-Estrany X, Simoes EAF, Dagan R, Hall CB, Harris B, Hultquist M, et al. Motavizumab for prophylaxis of respiratory syncytial virus in high-risk children: a noninferiority trial. Pediatrics. 2010;125(1):e35–51.

    Article  Google Scholar 

  19. 19.

    Walker EP. FDA Advisers Turn Down New RSV Drug.

  20. 20.

    Herschler B. 2010. ‘AstraZeneca drops lung drug and takes $445 million charge.’ Reuters.

    Google Scholar 

  21. 21.

    Taylor P. Regeneron drops RSV drug.

  22. 22.

    Mazur NI, Higgins D, Nunes MC, Melero JA, Langedijk AC, Horsley N, et al. The respiratory syncytial virus vaccine landscape: lessons from the graveyard and promising candidates. Lancet Infect Dis. 2018;18(10):295–311.

  23. 23.

    Teale A, Deshpande S, Burls A. Palivizumab and the importance of cost effectiveness. BMJ. 2009;338:b1935. Available from:

  24. 24.

    Piedimonte G, Perez MK. Role of early-life environmental influences in the development of asthma. How painful is it when you catch a bad cold too early? J ASTHMA. 2008;45(10):25–8.

    Article  Google Scholar 

  25. 25.

    Smart KA, Lanctot KL, Paes BA. The cost effectiveness of palivizumab: a systematic review of the evidence. J Med Econ. 2010;13(3):453–463. Available from:

  26. 26.

    Figueras-Aloy J, Carbonell-Estrany X, Quero J, Group IS. Case-control study of the risk factors linked to respiratory syncytial virus infection requiring hospitalization in premature infants born at a gestational age of 33-35 weeks in Spain. Pediatr Infect Dis J. 2004;23(9):815–820. Available from:

  27. 27.

    Higgins JPT, Green S, editors. Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0 [updated March 2011]. Bristol: The Cochrane Collaboration; 2011.

  28. 28.

    Deeks JJ, Higgins JPT, Altman DG, editors. Chapter 11: presenting results and ‘Summary of findings tables’. In: Cochrane Handbook for Systematic Reviews of Interventions. Version 5.1.0 (updated March 2011). Bristol: The Cochrane Collaboration; 2011. Available from:

  29. 29.

    Deeks JJ, Higgins JPT, Altman DG, editors. Chapter 12: interpreting results and drawing conclusions. In: Cochrane Handbook for Systematic Reviews of Interventions. Version 5.1.0 (updated March 2011). Bristol: The Cochrane Collaboration; 2011. Available from:

  30. 30.

    StatsDirect Ltd. StatsDirect statistical software. England: StatsDirect Ltd.; 2013.

    Google Scholar 

  31. 31.

    Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. BMJ. 2009;339 Available from:

  32. 32.

    Simoes EAF, Groothuis JR, Carbonell-Estrany X, Rieger CHL, Mitchell I, Fredrick LM, et al. Palivizumab prophylaxis, respiratory syncytial virus, and subsequent recurrent wheezing. J Pediatr. 2007;151(1):34–42.e1 United States. Available from:

    CAS  Article  Google Scholar 

  33. 33.

    O’Brien KL, Chandran A, Weatherholtz R, Jafri HS, Griffin MP, Bellamy T, et al. Efficacy of motavizumab for the prevention of respiratory syncytial virus disease in healthy Native American infants: a phase 3 randomised double-blind placebo-controlled trial. Lancet Infect Dis. 2015;15(12):1398–408 Available from: Donaldson C Perilla M, Campbell J, VanDeReit D, Brown LB, Gloyd PW, Seby M, Brown MA, Candelaria D, Foti JL, Overturf G E-CA, editor. United States.

    Article  Google Scholar 

  34. 34.

    Mochizuki H, Kusuda S, Okada K, Yoshihara S, Furuya H, Simoes EAF, et al. Palivizumab prophylaxis in preterm infants and subsequent recurrent wheezing. Six-year follow-up study. Am J Respir Crit Care Med. 2017;196(1):29–38. Available from: United States.

  35. 35.

    Carroll KN, Gebretsadik T, Escobar GJ, Wu P, Li SX, Walsh EM, et al. Respiratory syncytial virus immunoprophylaxis in high-risk infants and development of childhood asthma. J Allergy Clin Immunol. 2017;139(1):66–71.e3 United States. Available from:

    Article  Google Scholar 

  36. 36.

    Scheltema NM, Nibbelke EE, Pouw J, Blanken MO, Rovers MM, Naaktgeboren CA, et al. Respiratory syncytial virus prevention and asthma in healthy preterm infants: a randomised controlled trial. Lancet Respir Med. 2018;6(4):257–64. Available from:

    Article  Google Scholar 

  37. 37.

    Igde M, Kabasakal H, Ozturk O, Karatekin G, Aygun C, M. I, et al. Palivizumab prophylaxis, respiratory syncytial virus and subsequent development of asthma. Minerva Pediatr. 2018;70(3):252–9. Available from:

  38. 38.

    dos Santos Simões MC, Inoue Y, Matsunaga NY, Carvalho MR, Ribeiro GL, Morais EO, et al. Recurrent wheezing in preterm infants: prevalence and risk factors. J Pediatr (Rio J). 2019;95(6):720–7. Available from:

  39. 39.

    Moreno-Galdo A, Perez-Yarza EG, Ramilo O, Rubi T, Escribano A, Torres A, et al. Recurrent wheezing during the first 3 years of life in a birth cohort of moderate-to-late preterm infants. Pediatr Allergy Immunol. 2020;31(2):124–132.

  40. 40.

    Bockova J, O’Brien KL, Oski J, Croll J, Reid R, Weatherholtz RC, et al. Respiratory syncytial virus infection in Navajo and White Mountain Apache children. Pediatrics. 2002;110(2 Pt 1):e20.

    Article  Google Scholar 

  41. 41.

    Stockman LJ, Curns AT, Anderson LJ, Fischer-Langley G. Respiratory syncytial virus-associated hospitalizations among infants and young children in the United States, 1997-2006. Pediatr Infect Dis J. 2012;31(1):5–9.

    Article  Google Scholar 

  42. 42.

    Langley JM, Wang EE, Law BJ, Stephens D, Boucher FD, Dobson S, et al. Economic evaluation of respiratory syncytial virus infection in Canadian children: a Pediatric Investigators Collaborative Network on Infections in Canada (PICNIC) study. J Pediatr. 1997;131(1 Pt 1):113–7.

    CAS  Article  Google Scholar 

  43. 43.

    Shay DK, Holman RC, Newman RD, Liu LL, Stout JW, Anderson LJ. Bronchiolitis-associated hospitalizations among US children, 1980-1996. JAMA. 1999;282(15):1440–6.

    CAS  Article  Google Scholar 

  44. 44.

    Arnold SR, Wang EE, Law BJ, Boucher FD, Stephens D, Robinson JL, et al. Variable morbidity of respiratory syncytial virus infection in patients with underlying lung disease: a review of the PICNIC RSV database. Pediatric Investigators Collaborative Network on Infections in Canada. Pediatr Infect Dis J. 1999;18(10):866–9.

    CAS  Article  Google Scholar 

  45. 45.

    Thorburn K. Pre-existing disease is associated with a significantly higher risk of death in severe respiratory syncytial virus infection. Arch Dis Child. 2009;94(2):99–103.

  46. 46.

    Lenney W. The burden of pediatric asthma. Pediatr Pulmonol. 1997;24(S15):13–6.

  47. 47.

    Griffiths LJ, Lyons RA, Bandyopadhyay A, Tingay KS, Walton S, Cortina-Borja M, et al. Childhood asthma prevalence: cross-sectional record linkage study comparing parent-reported wheeze with general practitioner-recorded asthma diagnoses from primary care electronic health records in Wales. BMJ Open Respir Res. 2018;5(1):e000260.

    Article  Google Scholar 

  48. 48.

    Simoes EAF. Respiratory syncytial virus infection. Lancet. 1999;354(9181):847–52. Available from:

  49. 49.

    Blanken MO, Rovers MM, Molenaar JM, Winkler-Seinstra PL, Meijer A, Kimpen JLL, et al. Respiratory syncytial virus and recurrent wheeze in healthy preterm infants. N Engl J Med. 2013;368(19):1791–9.

    CAS  Article  Google Scholar 

  50. 50.

    Prais D, Kaplan E, Klinger G, Mussaffi H, Mei-Zahav M, Bar-Yishay E, et al. Short- and long-term pulmonary outcome of palivizumab in children born extremely prematurely. Chest. 2016;149(3):801–8.

    Article  Google Scholar 

  51. 51.

    Martinez FD, Wright AL, Taussig LM, Holberg CJ, Halonen M, Morgan WJ. Asthma and wheezing in the first six years of life. N Engl J Med [Internet]. 1995;332(3):133–8.

    CAS  Article  Google Scholar 

  52. 52.

    Simoes EAF, Carbonell-Estrany X, Rieger CHL, Mitchell I, Fredrick L, Groothuis JR, et al. The effect of respiratory syncytial virus on subsequent recurrent wheezing in atopic and nonatopic children. J Allergy Clin Immunol. 2010;126(2):256–62.

Download references


We acknowledge Richard Fallis, Queens University Belfast Medical Librarian, who kindly assisted with the development of the search strategy.


No source of funding was required for this systematic review.

Author information




All authors contributed to the search strategy, eligibility criteria, research question design and data analysis strategy. LAQ (first author) was the primary author involved in the writing of the review. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Lauren Alexandra Quinn.

Ethics declarations

Ethics approval and consent to participate

Not applicable

Consent for publication

Not applicable

Competing interests

HE Groves has delivered a presentation on her research at a non-promotional educational meeting and received honoria from Abbvie. All other authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1.

PRISMA 2009 Checklist.DOCX 19 kb)

Additional file 2.

Studies excluded based on full text, with full citation and reasoning.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Quinn, L.A., Shields, M.D., Sinha, I. et al. Respiratory syncytial virus prophylaxis for prevention of recurrent childhood wheeze and asthma: a systematic review. Syst Rev 9, 269 (2020).

Download citation


  • Respiratory syncytial virus
  • asthma
  • Recurrent wheeze
  • Prophylaxis
  • Monoclonal antibody
  • Immunoprophylaxis