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在南非进行的一项针对成人和新生儿的随机临床试验,旨在比较通过一次性注射器喷射注射器接种卡介苗(BCG)与使用针头和注射器的传统技术的安全性和免疫原性。

A randomized clinical trial in adults and newborns in South Africa to compare the safety and immunogenicity of bacille Calmette-Guérin (BCG) vaccine administration via a disposable-syringe jet injector to conventional technique with needle and syringe.

作者信息

Geldenhuys Hennie D, Mearns Helen, Foster Jennifer, Saxon Eugene, Kagina Benjamin, Saganic Laura, Jarrahian Courtney, Tameris Michele D, Dintwe One B, Van Rooyen Michele, Luabeya Kany-Kany A, Hussey Gregory, Scriba Thomas J, Hatherill Mark, Zehrung Darin

机构信息

South African Tuberculosis Vaccine Initiative (SATVI), Institute of Infectious Disease and Molecular Medicine (IDM) and Department of Paediatrics and Child Health, University of Cape Town, Brewelskloof Hospital, Haarlem Street, Worcester 6850, South Africa.

South African Tuberculosis Vaccine Initiative (SATVI), Institute of Infectious Disease and Molecular Medicine (IDM) and Department of Paediatrics and Child Health, University of Cape Town, Brewelskloof Hospital, Haarlem Street, Worcester 6850, South Africa.

出版信息

Vaccine. 2015 Sep 8;33(37):4719-26. doi: 10.1016/j.vaccine.2015.03.074. Epub 2015 Apr 7.

Abstract

INTRODUCTION

Intradermal bacille Calmette-Guérin (BCG) vaccination by needle-free, disposable-syringe jet injectors (DSJI) is an alternative to the Mantoux method using needle and syringe (NS). We compared the safety and immunogenicity of BCG administration via the DSJI and NS techniques in adults and newborn infants at the South African Tuberculosis Vaccine Initiative (SATVI) research site in South Africa.

METHOD

Thirty adults and 66 newborn infants were randomized 1:1 to receive intradermal BCG vaccine (0.1 mL in adults; 0.05 mL in infants) via DSJI or NS. Wheal diameter (mm) and skin fluid deposition at the site of injection (SOI) were measured immediately post-vaccination. Adverse events and SOI reactogenicity data were collected 30 min and 1, 2, 4, and 12 weeks after vaccination for adults and at 30 min and 4, 10, and 14 weeks for infants. Blood was collected in infants at 10 and 14 weeks to assess BCG-specific T-cell immune responses.

RESULTS

More infant BCG vaccinations by DSJI deposited >5 μL fluid on the skin surface, compared to NS (49% versus 9%, p=0.001). However, all 12 infant vaccinations that did not produce any SOI wheal occurred in the NS group (36%, p<0.001). Median wheal diameter, in participants for which an SOI wheal formed, did not differ significantly between groups in infants (combined 3.0mm IQR 2.0 to 4.0, p=0.59) or in adults (combined 9.0mm IQR 7.0 to 10.0, p=0.13). Adverse events were similar between study arms. Proportion of participants with BCG scars after three months did not differ in adults (combined 97%, p=0.67) or infants (combined 62%, p=0.13). Frequencies of BCG-specific clusters of differentiation 4 (CD4) and clusters of differentiation 8 (CD8) T-cells co-expressing IFN-γ, TNF-α, IL-2, and/or IL-17 were not different in the DSJI and NS groups.

CONCLUSION

BCG vaccination of newborn infants via DSJI was more likely to deliver an appropriate intradermal wheal at the SOI as compared to NS, despite leaving more fluid on the surface of the skin. Safety, reactogenicity, and antigen-specific T-cell immune responses did not differ between DSJI and NS techniques.

摘要

引言

使用无针一次性注射器喷射器(DSJI)进行皮内卡介苗(BCG)接种是一种替代使用针管注射器(NS)的结核菌素试验方法。我们在南非的南非结核病疫苗倡议(SATVI)研究地点比较了通过DSJI和NS技术在成人和新生儿中接种BCG的安全性和免疫原性。

方法

30名成人和66名新生儿按1:1随机分组,通过DSJI或NS接受皮内BCG疫苗接种(成人为0.1mL;婴儿为0.05mL)。接种疫苗后立即测量注射部位(SOI)的风团直径(mm)和皮肤液体沉积量。在成人接种疫苗后30分钟、1、2、4和12周以及婴儿接种疫苗后30分钟、4、10和14周收集不良事件和SOI反应原性数据。在婴儿10周和14周时采集血液,以评估BCG特异性T细胞免疫反应。

结果

与NS相比,通过DSJI接种BCG的婴儿在皮肤表面沉积>5μL液体的情况更多(49%对9%,p=0.001)。然而,所有12例未产生任何SOI风团的婴儿接种均发生在NS组(36%,p<0.001)。在形成SOI风团的参与者中,婴儿组(合并3.0mm,四分位间距2.0至4.0,p=0.59)或成人组(合并9.0mm,四分位间距7.0至10.0,p=0.13)的风团直径中位数在两组之间无显著差异。研究组之间的不良事件相似。三个月后有BCG疤痕的参与者比例在成人(合并97%,p=0.67)或婴儿(合并62%,p=0.13)中无差异。DSJI组和NS组中共同表达IFN-γ、TNF-α、IL-2和/或IL-17的BCG特异性分化簇4(CD4)和分化簇8(CD8)T细胞频率无差异。

结论

与NS相比,通过DSJI对新生儿进行BCG接种更有可能在SOI处形成合适的皮内风团,尽管在皮肤表面留下了更多液体。DSJI和NS技术在安全性、反应原性和抗原特异性T细胞免疫反应方面没有差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa61/4564069/72508e9d92a0/mmc1.jpg

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