Oral polio vaccine (OPV) is recommended to be given at birth together with BCG vaccine. While we were conducting two trials including low-birth-weight (LBW) and normal-birth-weight (NBW) infants in Guinea-Bissau, OPV was not available during some periods and therefore some infants did not receive OPV at birth, but only BCG. We investigated the effect of OPV given simultaneously with BCG at birth on the immune response to BCG vaccine.
Methods and Findings
We compared the in vitro and the in vivo response to PPD in the infants who received OPV and BCG with that of infants who received BCG only. At age 6 weeks, the in vitro cytokine response to purified protein derivate (PPD) of M. Tuberculosis was reduced in LBW and NBW infants who had received OPV with BCG. In a pooled analysis receiving OPV with BCG at birth was associated with significantly lower IL-13 (p = 0.041) and IFN-γ (p = 0.004) and a tendency for lower IL-10 (p = 0.054) in response to PPD. Furthermore, OPV was associated with reduced in vivo response to PPD at age 2 months, the prevalence ratio (PR) of having a PPD reaction being 0.75 (0.58–0.98), p = 0.033, and with a tendency for reduced likelihood of having a BCG scar (0.95 (0.91–1.00), p = 0.057)). Among children with a scar, OPV was associated with reduced scar size, the regression coefficient being −0.24 (−0.43—0.05), p = 0.012.
This study is the first to address the consequences for the immune response to BCG of simultaneous administration with OPV. Worryingly, the results indicate that the common practice in low-income countries of administering OPV together with BCG at birth may down-regulate the response to BCG vaccine.
Citation: Sartono E, Lisse IM, Terveer EM, van de Sande PJM, Whittle H, Fisker AB, et al. (2010) Oral Polio Vaccine Influences the Immune Response to BCG Vaccination. A Natural Experiment. PLoS ONE 5(5): e10328. https://doi.org/10.1371/journal.pone.0010328
Editor: Lisa F. P. Ng, Singapore Immunology Network, Singapore
Received: December 18, 2009; Accepted: April 2, 2010; Published: May 21, 2010
Copyright: © 2010 Sartono et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The study was supported by the European Commission, INCO-programme (contract no. ICA4-CT-2002-10053). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
WHO recommends BCG vaccine and oral polio vaccine (OPV) at birth in low-income countries. BCG vaccine is the world's most widely used vaccine and although its efficacy is variable, it is still considered the best way to protect against childhood tuberculosis , . BCG vaccination induces potent Th1 responses to mycobacterial antigen in newborns . Studies in Gambia have shown that BCG vaccination affects responses to unrelated vaccines by enhancing the production of Th1 and Th2 type cytokines , . BCG vaccination in early life also increased the antibody response to OPV . The effect of providing OPV simultaneously with BCG on the immune response to BCG has never been studied.
We recently conducted two trials among newborns in Guinea-Bissau. According to local practice, low-birth-weight (LBW, <2500 g) infants only receive OPV at birth; BCG vaccine is usually postponed until the child reaches 6 weeks of age. In trial 1, LBW infants were randomized to receive an early BCG vaccine or the usual delayed BCG vaccine. In trial 2, normal birth-weight (NBW, ≥2500 g) children were randomized to vitamin A supplementation or placebo together with BCG vaccine . The children were followed for mortality. Subgroups of the children were also followed for the in vivo and in vitro immune response to BCG . OPV is recommended to be given at birth but for certain periods in 2004, during the conduct of the two trials, OPV was not available in Guinea-Bissau and hence some trial participants did not receive OPV at birth. This ‘natural experiment’ allowed us to compare in an observational, but rather unbiased manner, the effect of OPV provided with BCG at birth. Intriguingly, we observed that not receiving OPV at birth was associated with significantly decreased male mortality during the first year of life . In the present study we investigated the effect of OPV given simultaneously with BCG at birth on the immune response to BCG vaccine.
Materials and Methods
This study was conducted according to the principles expressed in the Declaration of Helsinki. The study was approved by the research committee of the Ministry of Health in Guinea-Bissau and for European Centers by the Danish Central Ethical Committee. All mothers provided written informed consent for the collection of samples of their children.
The two large randomized trials were conducted by the Bandim Health Project (BHP) in Bissau, Guinea-Bissau. The BHP covers a population of around 100,000 in 6 districts in the urban area by a demographic surveillance system. All houses are visited every month to register new pregnancies and births. Once a newborn is identified, the child is followed with a home visit every third month. There is a national hospital (NH) with a maternity ward in the capital and three health centers in the study area, one of them with a maternity ward. Around 60–70% of the mothers from the study area deliver at the NH or at the health center maternity ward. Since 2002 all LBW infants born at the NH have been followed for one year, also infants outside the study area. In trial 1, all LBW infants born at the NH or in the study area were invited to participate in a trial studying the effect of receiving early BCG vaccination on mortality and cytokine levels in LBW infants. In trial 2, NBW infants from the study area were invited to participate in a trial studying the effect of vitamin A supplementation at birth on mortality and cytokine levels. These two EU funded trials were carried out within a collaborative network of European and Guinea-Bissau institutions. The trials were registered at www.clinicaltrials.gov, registration number, NCT00146302 and NCT00168597.
Enrolment into the trials
Newborns were enrolled throughout 2004 (Figure 1). Mothers were informed of the purpose of the study. If a mother of a LBW infant accepted to participate, she drew a randomization number indicating whether the children would be BCG vaccinated early or not. If a mother of a NBW infant accepted to participate, she drew a randomization number indicating whether the children would receive vitamin A supplementation (50,000 IU) or placebo. At the time of enrolment, children were examined clinically. The infants were weighed and length, head-circumference and mid-upper-arm-circumference (MUAC) were measured. Newborns that were overtly ill were not enrolled but referred to treatment.
LBW infants who were randomized to not receiving early BCG vaccination were not included in the present study since we aimed to look at the effect of OPV on the immune response to BCG given at the same time. Hence, the LBW population only includes children who were randomized to BCG at birth. NBW children who had received vitamin A supplementation at birth were not included in the present study as this could have affected their response to OPV and BCG. Hence, the NBW population only includes children who were randomized to placebo at birth.
BCG (0.05 ml; Statens Serum Institut, Copenhagen, Denmark) was provided by the BHP and given intradermally in the upper left deltoid region. OPV was supplied through the national immunization programme and given orally. Three types of OPV were used in Guinea-Bissau, produced by Novartis, Sanofi Pasteur, and GlaxoSmithKline. However, OPV was missing during periods of 2004. As part of our trial routines, we noted at the inclusion form whether the children received OPV or not. Based on the distribution of children who had not received OPV, OPV was missing at one or more inclusion sites 1) from the beginning of February 2004 to the beginning of June 2004, 2) again in the end of June 2004, and 3) from the end of October 2004 to November 2004 (Figure 1).
Follow-up for in vitro PPD response
We aimed to enroll 200 children from trial 1 and 400 children from trial 2 in a subgroup study of cytokine production. The children were enrolled between April and November 2004 (Figure 1). We attempted to visit the children at 6 weeks of age. A blood sample was collected by finger prick and analyzed for in vitro cytokine responses. Whole blood cultures were done as previously described , . Briefly, heparinized finger prick blood was diluted in RPMI 1640 medium (Invitrogen, Breda, The Netherlands) to a final concentration of 1 in 10 and culture in a total volume of 200 µl in 96-well U plate (Nunc, Roskilde, Denmark) with the presence of purified protein derivative of Mycobacterium tuberculosis (PPD, 10 µg/ml; Statens Serum Institut, Denmark, Copenhagen). Supernatants were collected on day 3 and stored at −80°C.
Measurement of cytokine levels
IL-5, IL-10, IL-13, IFN-γ and TNF-α from day 3 supernatants were analyzed simultaneously using commercial Luminex cytokine kit and buffer reagent kit (BioSource, Camarillo, CA, USA) and run on a Luminex-100 cytometer (Luminex Corporation, Austin, TX, USA), equipped with StarStation software (Applied Cytometry Systems, Dinnington, UK). The assay was performed with slight modification from the manufacturer's recommendation. Briefly, assays were done in a 96-well U plate at room temperature. Mixes of beads were incubated for 2 hours with a standard, samples, or blank in a final volume of 50 µl for 2 hours under continuous shaking. Beads were washed twice and incubated with cocktail of biotinylated antibodies (25 µl/well) for 1 hour. After removal of excess biotinylated antibodies, Streptavidin-PE was added for 30 minutes. The plate was then washed and analyzed. The lower detection limit of the assays was 3 pg/ml, 5 pg/ml, 10 pg/ml, 5 pg/ml and 10 pg/ml for IL-5, IL-10, IL-13, IFN-γ and TNF-α, respectively. Samples with concentrations below the detection limit were given the value of this threshold.
Follow-up for BCG scar and in vivo PPD response
All LBW children were visited at home and examined for BCG scar and in vivo PPD response at 2 and 6 months of age. In four of six study area districts NBW children were examined for BCG scar and in vivo PPD response when they reached 2 and 6 months of age. At the home visits a trained nurse documented health status and vaccination status. She measured the size of the scar following BCG vaccination. Subsequently, 0.1 ml of Tuberculin PPD RT23 (Statens Serum Institut, Copenhagen, Denmark) was injected intradermally on the ventral side of the forearm. Between 48 and 72 hours later, the child was visited again, and the induration was measured by a trained field worker using track-ball technique . Size of scar and induration was defined as the average of the height and the width measured to nearest millimeter with a transparent ruler. Children with a measurable scar were categorized as “scar-positive”. Children with a mean diameter of the induration ≥2 mm were categorized as “PPD-positive”. Children who had taken chloroquine within seven days prior to the visit were excluded from the PPD analysis, since chloroquine treatment is known to suppress PPD reaction . These children were retained in the analysis of scar reaction since we considered it unlikely that current chloroquine treatment would have affected the scar formation. Children who had received BCG vaccination less than 30 days prior to the visit or with known exposure to tuberculosis in the household within the previous 6 months (information only available for NBW population) were excluded. Children with PPD reactions >10 mm were referred to a medical doctor to be further examined for tuberculosis (TB).
All statistical analysis was performed in Stata 10.0.
In vitro PPD response.
Cytokine levels were not normally distributed. The crude cytokine levels were first compared in a univariate analysis using non-parametric Mann-Whitney U tests, and the results were provided in the figures of the distribution of cytokine levels in the different groups (Figures 2 and 3). Subsequently, the frequency of low and high cytokine producers in BCG and BCG+OPV recipients was compared in Poisson regression model with robust variance estimates  using the median cytokine level in the total population as cut off for low and high responder. Thus, the relative measure is a prevalence ratio (PR). The study population was divided into 4 groups according to the birth weight and whether OPV was given together with BCG at birth (Table 1). As the periods with lack of OPV fell primarily in the dry season (from December to May), all children who had received BCG+OPV had been vaccinated in the rainy season (June to November). The two LBW groups were similar with respect to age and sex. However, MUAC at enrolment was larger in the BCG+OPV group compared with the BCG group, and they had received more OPV and more diphtheria-tetanus-pertussis (DTP) vaccines (recommended at age 6, 10 and 14 weeks) between enrolment and blood sampling (Table 1). The two NBW groups were similar with respect to age and MUAC at enrolment (Table 1). However, they were significantly different with regard to sex, the NBW BCG+OPV group having fewer boys. The two groups also differed significantly with regard to vaccinations received between enrolment and blood sampling (more OPV and less DTP in the BCG+OPV group). All further analyses were adjusted for age, sex, month of enrolment, MUAC at enrolment, and vaccinations between enrolment and blood sampling.
One dot represents one individual. Horizontal lines represent medians.
One dot represents one individual. Horizontal lines represent medians.
BCG scar and in vivo PPD response.
PPD response (yes/no) and scar response (yes/no) were analyzed as prevalence data using a Poisson regression model with robust variance estimates providing prevalence ratios (PR) . Children with a PPD response above 15 mm were excluded from the analyses as they had potentially been exposed to TB. There were no such children among LBW children. Among NBW children one boy (BCG+OPV) had a PPD response above 15 mm at age 2 months and was excluded from further analyses. At age 6 months, one boy (BCG+OPV) and one girl (BCG), had a PPD response above 15 mm and were excluded from the 6 month-analysis. As in the cytokine analysis, there was a clear overweight of children who had received BCG+OPV in the rainy season, though there was more variation because the follow-up for PPD/scar had been conducted throughout 2004 (Figure 1). Among LBW infants, the BCG+OPV recipients only differed from the BCG only recipients with regard to season (Table 2). Among NBW infants, the two groups also differed with regard to MUAC at enrolment, and number of OPV received between enrolment and the PPD/Scar assessment (Table 2). We adjusted the analyses for sex, season (the larger variation in this analysis compared with the cytokine analysis allowed us to control for season rather than month), MUAC, and subsequent vaccinations. As in previous studies of PPD responses, the reading of the PPD reaction differed significantly by the assistant doing the reading and the analyses of PPD responses were therefore furthermore adjusted for assistant. Among PPD responders and/or scar reactors, we analyzed the size of the reaction in linear regression models controlling for the same potential confounders.
In vitro PPD response
This analysis included 61 LBW infants who had been randomized to early BCG; 33 who had not received OPV at birth together with BCG and 28 who had. Furthermore, 248 NBW infants who had been randomized to placebo; 69 who had not received OPV and 179 who had were included.
Influence of OPV on cytokine responses to PPD in LBW infants
When OPV was given together with BCG, there was a significant down regulation of IL-5, IL-13, and IFN-γ in response to PPD as compared to the group of infants who had received BCG only (Figure 2)(Table 3). IL-10 to PPD was higher in LBW infants who had received BCG together with OPV in the crude analysis, but the difference disappeared in the adjusted analysis (Table 3). There were no significant differences in TNF-α to PPD between the two groups (Figure 2)(Table 3).
Influence of OPV on cytokine responses to PPD in NBW infants
In the unadjusted analysis IFN-γ responses to PPD appeared depressed and IL-10 responses increased when OPV was given with BCG (Figure 3). In the adjusted analysis, the IFN-γ levels to PPD were significantly lower in BCG+OPV compared with BCG only vaccinated infants and there was a similar tendency for IL-13 (Table 3).
Influence of OPV on cytokine responses to PPD in all infants
In a pooled analysis of LBW and NBW infants, receiving OPV with BCG at birth was associated with significantly lower IL-13 and IFN-γ in responses to PPD; the adjusted PRs (furthermore adjusted for being LBW) were 0.64 (0.41–0.98)(p = 0.041), and 0.51 (0.33–0.80)(p = 0.004), respectively. The IL-10 response to PPD tended to be lower as well (0.61 (0.36–1.01), p = 0.054).
BCG scar and in vivo PPD response
Among LBW infants enrolled in 2004, 250 BCG recipients were visited; 104 had received BCG+OPV, 146 BCG only. We obtained a scar reading in 231 children at age 2 months and 200 children at age 6 months and a valid PPD assessment of 202 at age 2 months, and 170 at age 6 months. Among NBW infants enrolled in 2004, 540 placebo recipients had their BCG scar and PPD response assessed once or more; 287 had received BCG+OPV; 253 BCG only. We obtained a scar reading in 438 children at age 2 months and 428 children at age 6 months and a valid PPD assessment of 379 at age 2 months, and 327 at age 6 months.
Influence of OPV on PPD/Scar responses in LBW infants.
At age 2 months, receiving OPV with BCG at birth was associated with a borderline significantly lower likelihood of being PPD positive (Table 4). There was no association with size of the reaction among the few children who had a positive reaction. Almost all children were scar positive, and there was no association between OPV at birth and being scar positive (Table 5), or the size of the scar among scar positives (data not shown).
At age 6 months, the lower likelihood of being PPD positive (Table 4) was no longer significant for the OPV group and there was no association with size of the reaction among the few children who had a positive reaction. Almost all children were scar positive, and there was no association between OPV at birth and being scar positive (Table 5), or the size of the scar among scar positives (data not shown).
Influence of OPV on PPD/Scar responses in NBW infants.
At age 2 months, receiving OPV with BCG at birth was not associated with the likelihood of being PPD positive (Table 4), nor was it associated with the size of the response among children with a positive response (data not shown). Adjusted for potential confounders, children who had received OPV at birth had a lower likelihood of developing a BCG scar (Table 5). Receiving OPV at birth was negatively associated with the size of the scar among those who had a scar (regression coefficient −0.36 (−0.57—0.15); p = 0.001).
At age 6 months, receiving OPV with BCG at birth was not associated with the likelihood of being PPD positive (Table 4) or the size of the PPD reaction (data not shown). Almost all children had a scar at age 6 months and receiving OPV at birth was not associated with the likelihood of being scar positive (Table 5) or the size of the scar (data not shown).
Influence of OPV on PPD/Scar responses in all infants.
In a pooled analysis of LBW and NBW infants, receiving OPV with BCG at birth was associated with significantly lower likelihood of being PPD positive at age 2 months, the PR being 0.75 (0.58–0.98), p = 0.033. OPV with BCG was not associated with size of the PPD reaction (data not shown). OPV with BCG was also tended to be associated with a reduced likelihood of being scar positive (0.95 (0.91–1.00), p = 0.057). Among scar positive children, OPV was associated with significantly reduced scar size, the regression coefficient being −0.24 (−0.43—0.05), p = 0.012 (Figure 4). No significant differences were seen at age 6 months.
This study is the first to demonstrate that mucosal administration of OPV simultaneously with intradermal BCG vaccination may have profound immunological consequences. By comparing immune responses of infants who had received BCG at birth either with or without OPV, we observed that OPV had a significant suppressing effect on Th1 and Th2 responses to PPD. These in vitro findings were paralleled by findings of significantly reduced in vivo responses to PPD, a tendency for less BCG scars, and significantly reduced BCG scar size among those who developed a scar.
Strengths and weaknesses
Though OPV is widely used, little is known regarding the cellular immune responses following vaccination, in particular its non-specific immune responses to un-related stimuli. The effect of OPV could be studied in the present study due to a temporary shortage of the vaccine in Guinea-Bissau during several periods of 2004. The shortage occurred in a period when two trials, examining among other things the immune responses of newborns, were being conducted. It was therefore possible to study in a relatively unbiased manner the effect of OPV on the in vitro response to PPD, as well as the effect on two markers of BCG immunity: PPD responses and BCG scarification.
Strengths of our study include the design; it was mainly logistic factors which determined whether the children would receive OPV or not. Despite this, there were some clear differences between the children who did or did not receive OPV at birth for instance with regard to season of vaccination, anthropometrics at inclusion, and other vaccines received. We conducted our analyses with and without adjustment for these co-variables, and indeed noted that the crude estimated changed considerably when we included the other variables as evidence of confounding. We cannot exclude that there is considerable residual confounding due to for instance the burden of maternal infectious diseases, other vaccines received or nutritional status. Especially, residual confounding by season could be a problem. A recent study in Malawi found that in vitro IFN-γ response to PPD varied strongly by season, being lowest in the warm and rainy season as compared with the cool and dry season and the hot and dry season . In Guinea-Bissau there are two distinct seasons. Our periods without OPV coincided with the dry season. Hence, we have largely compared children who received OPV in the rainy season with children who received no OPV in the dry season. If the IFN-γ response to PPD was depressed for other reasons in the rainy season it could be at least part of the reason for the observed lower IFN-γ response to PPD response in OPV recipients. However, we found the same results when we limited our analysis to the rainy season, though the confidence intervals of course became wider (data not shown). Furthermore, we found depressed in vivo responses to PPD as well. The PPD data set was larger than the cytokine data set, and had more seasonal variation and thereby more power to control adequately for season. The validity of our findings is supported by the fact that the findings from the LBW and NBW cohorts consistently pointed in the same direction, and the pooled analyses provided significant results. Nonetheless, our findings should be interpreted with caution.
Previously, it has been shown that BCG vaccination given at birth in either NBW or LBW infants enhanced immune response to PPD, characterized by elevated IL-5, IL-13 and IFN-γ levels (4, and unpublished data). In the present study, the administration of OPV at the time of BCG priming at birth, reduced Th1 and Th2 cytokine responses to mycobacterial antigens in LBW infants, suggesting that OPV down regulated cellular immune responses to BCG vaccine when the vaccines were administrated at the same time.
One possible mechanism whereby OPV co administered with BCG leads to a reduced cellular response to PPD may be competition of OPV and BCG activated T cells for resources and space , . A second possible mechanism is that polio virus may have specific immune modulatory molecules that down regulate immune responses to antigens to which immune responses are being mounted simultaneously .
The fact that the downregulation of cytokine production to PPD as a result of OPV vaccination was more profound in LBW compared to NBW infants might be due to functional immaturity of LBW infants. A recent study by Klein et al. showed that after inactivated polio vaccine, preterm infants had comparable frequencies of poliovirus specific CD4+CD45RO+CD69+IFN-γ memory T cells but diminished lymphoproliferation compared to term infants . Furthermore, it is also possible the differences between LBW and NBW infants were caused by differences in the genetic make up. A study by Anuradha et al. reported that IFN-γ low producer genotype +874T/A were over represented in BCG non-responding children .
Implications for BCG immunity
There is considerable evidence, both in humans and animals that IFN-γ production is necessary for protective immunity against mycobacterial disease – and successful chemotherapy of TB is associated with augmented IFN-γ production –. Furthermore, it has also been reported that individuals with genetic abnormalities of the IFN-γ receptor are highly susceptible to intracellular infections –. Thus, immunity to tuberculosis might be impaired by the down regulation of this Th1 response in LBW children receiving OPV at the same time as BCG at birth. The finding is supported by the fact that we found reduced PPD responses and reduced BCG scarification and scar size at age 2 months although these are debatable markers for TB immunity. Interestingly, the differences were no longer significant at age 6 months. It could be speculated that the PPD skin test at 2 months of age boosted the immune response to BCG and this obliterated the differences at 6 months. It has previously been reported that PPD skin test boosts the subsequent skin test reactivity . The clinical implications of this early depression in immune responses to BCG need to be addressed in well-designed randomized trials with sufficient follow-up.
It is worth noticing that the protection induced by BCG against tuberculosis has been found to be much higher in high-income countries than in low-income countries. High-income countries mainly administer inactivated polio vaccine (IPV) at several months of age. Though many of the BCG-efficacy studies were done many years ago, before the introduction of OPV at birth, it may be speculated that the addition of OPV to BCG at birth has further compromised the protection induced by BCG in low-income countries.
In summary, we are aware that the study population is small, and though we were able to control for a number of confounders there may be residual confounding. However, the potential effect of OPV on the immune response to BCG vaccine has not been studied before, and it may seem biologically plausible that the two vaccines interact with each other. The potentially negative effect of OPV on the immune response to BCG vaccine should be tested in a randomized trial.
We are indebted to all study participants at the Bandim Health Project (BHP) in Bissau, Guinea-Bissau.
Conceived and designed the experiments: HCW PA MY. Performed the experiments: ES IML EMT PJMvdS ABF AR CSB. Analyzed the data: ES IML ABF AR CSB. Wrote the paper: ES CSB.
- 1. Colditz GA, Brewer TF, Berkey CS, Wilson ME, Burdick E, et al. (1994) Efficacy of BCG vaccine in the prevention of tuberculosis. Meta-analysis of the published literature. JAMA 271: 698–702.GA ColditzTF BrewerCS BerkeyME WilsonE. Burdick1994Efficacy of BCG vaccine in the prevention of tuberculosis. Meta-analysis of the published literature.JAMA271698702
- 2. Fine PE (1995) Variation in protection by BCG: implications of and for heterologous immunity. Lancet 346: 1339–45.PE Fine1995Variation in protection by BCG: implications of and for heterologous immunity.Lancet346133945
- 3. Marchant A, Goetghebuer T, Ota MO, Wolfe I, Ceesay SJ, et al. (1999) Newborns develop a Th1-type immune response to Mycobacterium bovis bacillus Calmette-Guérin vaccination. J Immunol 163: 2249–55.A. MarchantT. GoetghebuerMO OtaI. WolfeSJ Ceesay1999Newborns develop a Th1-type immune response to Mycobacterium bovis bacillus Calmette-Guérin vaccination.J Immunol163224955
- 4. Ota MO, Vekemans J, Schlegel-Haueter SE, Fielding K, Sanneh M, et al. (2002) Influence of Mycobacterium bovis bacillus Calmette-Guérin on antibody and cytokine responses to human neonatal vaccination. J Immunol 168: 919–25.MO OtaJ. VekemansSE Schlegel-HaueterK. FieldingM. Sanneh2002Influence of Mycobacterium bovis bacillus Calmette-Guérin on antibody and cytokine responses to human neonatal vaccination.J Immunol16891925
- 5. Benn CS, Diness BR, Roth A, Nante E, Fisker AB, et al. (2008) Effect of 50,000 IU vitamin A given with BCG vaccine on mortality in infants in Guinea-Bissau: randomised placebo controlled trial. BMJ 336: 1416–20.CS BennBR DinessA. RothE. NanteAB Fisker2008Effect of 50,000 IU vitamin A given with BCG vaccine on mortality in infants in Guinea-Bissau: randomised placebo controlled trial.BMJ336141620
- 6. Diness BR, Fisker AB, Roth A, Yazdanbakhsh M, Sartono E, et al. (2007) Effect of high-dose vitamin A supplementation on the immune response to Bacille Calmette-Guerin vaccine. Am J Clin Nutr 86: 1152–9.BR DinessAB FiskerA. RothM. YazdanbakhshE. Sartono2007Effect of high-dose vitamin A supplementation on the immune response to Bacille Calmette-Guerin vaccine.Am J Clin Nutr8611529
- 7. Benn CS, Fisker AB, Rodrigues A, Ravn H, Sartono E, et al. (2008) Sex-differential effect on infant mortality of oral polio vaccine administered with BCG at birth in Guinea-Bissau. A natural experiment. PLoS ONE 3(12): e4056.CS BennAB FiskerA. RodriguesH. RavnE. Sartono2008Sex-differential effect on infant mortality of oral polio vaccine administered with BCG at birth in Guinea-Bissau. A natural experiment.PLoS ONE3(12)e4056
- 8. Eriksson M, Sartono E, Martins CL, Balé C, Garly ML, et al. (2007) A comparison of ex vivo cytokine production in venous and capillary blood. Clin Exp Immunol 150: 469–76.M. ErikssonE. SartonoCL MartinsC. BaléML Garly2007A comparison of ex vivo cytokine production in venous and capillary blood.Clin Exp Immunol15046976
- 9. Bouros D, Zeros G, Panaretos C, Vassilatos C, Siafakas N (1999) Palpation vs pen method for the measurement of skin tuberculin reaction (Mantoux test). Chest 99: 416–9.D. BourosG. ZerosC. PanaretosC. VassilatosN. Siafakas1999Palpation vs pen method for the measurement of skin tuberculin reaction (Mantoux test).Chest994169
- 10. Garly ML, Bale C, Martins CL, Baldé MA, Hedegaard KL, et al. (2001) BCG vaccination among West African infants is associated with less anergy to tuberculin and diphtheria-tetanus antigens. Vaccine 20: 468–74.ML GarlyC. BaleCL MartinsMA BaldéKL Hedegaard2001BCG vaccination among West African infants is associated with less anergy to tuberculin and diphtheria-tetanus antigens.Vaccine2046874
- 11. Barros AJ, Hirakata VN (2003) Alternatives for logistic regression in cross-sectional studies: an empirical comparison of models that directly estimate the prevalence ratio. BMC Med Res Methodol 3: 21.AJ BarrosVN Hirakata2003Alternatives for logistic regression in cross-sectional studies: an empirical comparison of models that directly estimate the prevalence ratio.BMC Med Res Methodol321
- 12. Lalor MK, Ben-Smith A, Gorak-Stolinska P, Weir RE, Floyd S, et al. (2009) Population differences in immune responses to Bacille Calmette-Guérin vaccination in infancy. J Infect Dis 199: 795–800.MK LalorA. Ben-SmithP. Gorak-StolinskaRE WeirS. Floyd2009Population differences in immune responses to Bacille Calmette-Guérin vaccination in infancy.J Infect Dis199795800
- 13. Günther J, Haas W, Von Boehmer H (1982) Suppression of T cell responses through competition for T cell growth factor (interleukin 2). Eur J Immunol 12: 247–9.J. GüntherW. HaasH. Von Boehmer1982Suppression of T cell responses through competition for T cell growth factor (interleukin 2).Eur J Immunol122479
- 14. Stockinger B, Kassiotis G, Bourgeois C (2004) CD4 T-cell memory. Semin Immunol 16: 295–303.B. StockingerG. KassiotisC. Bourgeois2004CD4 T-cell memory.Semin Immunol16295303
- 15. Vekemans J, Ota MO, Wang EC, Kidd M, Borysiewicz LK, et al. (2002) T cell responses to vaccines in infants: defective IFNgamma production after oral polio vaccination. Clin Exp Immunol 127: 495–8.J. VekemansMO OtaEC WangM. KiddLK Borysiewicz2002T cell responses to vaccines in infants: defective IFNgamma production after oral polio vaccination.Clin Exp Immunol1274958
- 16. Klein NP, Gans HA, Sung P, Yasukawa LL, Jhonson J, et al. (2010) Preterm infants' T cell responses to inactivated poliovirus vaccine. J Infect Dis 201: 214–22.NP KleinHA GansP. SungLL YasukawaJ. Jhonson2010Preterm infants' T cell responses to inactivated poliovirus vaccine.J Infect Dis20121422
- 17. Anuradha B, Rakh SS, Ishaq M, Murthy KJR, Valluri VL (2008) Interferon-γ low producer genotype +874 overrepresented in Bacillus Calmette-Guirin nonresponding children. Pediatr Infect Dis J 27: 325–9.B. AnuradhaSS RakhM. IshaqKJR MurthyVL Valluri2008Interferon-γ low producer genotype +874 overrepresented in Bacillus Calmette-Guirin nonresponding children.Pediatr Infect Dis J273259
- 18. Cooper AM, Dalton DK, Stewart TA, Griffin JP, Russell DG, et al. (1993) Disseminated tuberculosis in interferon gamma gene-disrupted mice. J Exp Med 178: 2243–7.AM CooperDK DaltonTA StewartJP GriffinDG Russell1993Disseminated tuberculosis in interferon gamma gene-disrupted mice.J Exp Med17822437
- 19. Flynn JL, Chan J, Triebold KJ, Dalton DK, Stewart TA, et al. (1993) An essential role for interferon gamma in resistance to Mycobacterium tuberculosis infection. J Exp Med 178: 2249–54.JL FlynnJ. ChanKJ TrieboldDK DaltonTA Stewart1993An essential role for interferon gamma in resistance to Mycobacterium tuberculosis infection.J Exp Med178224954
- 20. Jouanguy E, Altare F, Lamhamedi S, Revy P, Emile JF, et al. (1996) Interferon-gamma-receptor deficiency in an infant with fatal bacille Calmette-Guérin infection. N Engl J Med 335: 1956–61.E. JouanguyF. AltareS. LamhamediP. RevyJF Emile1996Interferon-gamma-receptor deficiency in an infant with fatal bacille Calmette-Guérin infection.N Engl J Med335195661
- 21. Newport MJ, Huxley CM, Huston S, Hawrylowicz CM, Oostra BA, et al. (1996) A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infection. N Engl J Med 335: 1941–9.MJ NewportCM HuxleyS. HustonCM HawrylowiczBA Oostra1996A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infection.N Engl J Med33519419
- 22. Al-Attiyah R, Mustafa AS, Abal AT, Madi NM, Andersen P (2003) Restoration of mycobacterial antigen-induced proliferation and interferon-gamma responses in peripheral blood mononuclear cells of tuberculosis patients upon effective chemotherapy. FEMS Immunol Med Microbiol 38: 249–56.R. Al-AttiyahAS MustafaAT AbalNM MadiP. Andersen2003Restoration of mycobacterial antigen-induced proliferation and interferon-gamma responses in peripheral blood mononuclear cells of tuberculosis patients upon effective chemotherapy.FEMS Immunol Med Microbiol3824956
- 23. Hirsch CS, Toossi Z, Othieno C, Johnson JL, Schwander SK, et al. (1999) Depressed T-cell interferon-gamma responses in pulmonary tuberculosis: analysis of underlying mechanisms and modulation with therapy. J Infect Dis 180: 2069–73.CS HirschZ. ToossiC. OthienoJL JohnsonSK Schwander1999Depressed T-cell interferon-gamma responses in pulmonary tuberculosis: analysis of underlying mechanisms and modulation with therapy.J Infect Dis180206973
- 24. Marchant A, Amedei A, Azzurri A, Vekemans J, Benagiano M, et al. (2001) Polarization of PPD-specific T-cell response of patients with tuberculosis from Th0 to Th1 profile after successful antimycobacterial therapy or in vitro conditioning with interferon-alpha or interleukin-12. Am J Respir Cell Mol Biol 24: 187–94.A. MarchantA. AmedeiA. AzzurriJ. VekemansM. Benagiano2001Polarization of PPD-specific T-cell response of patients with tuberculosis from Th0 to Th1 profile after successful antimycobacterial therapy or in vitro conditioning with interferon-alpha or interleukin-12.Am J Respir Cell Mol Biol2418794
- 25. Allende LM, López-Goyanes A, Paz-Artal E, Corell A, García-Pérez MA, et al. (2001) A point mutation in a domain of gamma interferon receptor 1 provokes severe immunodeficiency. Clin Diagn Lab Immunol 8: 133–7.LM AllendeA. López-GoyanesE. Paz-ArtalA. CorellMA García-Pérez2001A point mutation in a domain of gamma interferon receptor 1 provokes severe immunodeficiency.Clin Diagn Lab Immunol81337
- 26. Cunningham JA, Kellner JD, Bridge PJ, Trevenen CL, Mcleod DR, et al. (2000) Disseminated bacille Calmette-Guérin infection in an infant with a novel deletion in the interferon-gamma receptor gene. Int J Tuberc Lung Dis 4: 791–4.JA CunninghamJD KellnerPJ BridgeCL TrevenenDR Mcleod2000Disseminated bacille Calmette-Guérin infection in an infant with a novel deletion in the interferon-gamma receptor gene.Int J Tuberc Lung Dis47914
- 27. Dorman SE, Holland SM (1998) Mutation in the signal-transducing chain of the interferon-gamma receptor and susceptibility to mycobacterial infection. J Clin Invest 101: 2364–9.SE DormanSM Holland1998Mutation in the signal-transducing chain of the interferon-gamma receptor and susceptibility to mycobacterial infection.J Clin Invest10123649
- 28. Dogan E, Erkoc R, Sayarlioglu H, Uzun K (2005) Tuberculin skin test results and the booster phenomenon in two-step tuberculin skin testing in hemodialysis patients. Ren Fail 27: 425–8.E. DoganR. ErkocH. SayarliogluK. Uzun2005Tuberculin skin test results and the booster phenomenon in two-step tuberculin skin testing in hemodialysis patients.Ren Fail274258