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Factors influencing secondary vibriocidal immune responses: relevance for understanding immunity to cholera.

机译:影响继发杀线免疫反应的因素:了解霍乱免疫力的相关性。

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摘要

Although serum vibriocidal activity is used extensively as a marker of immunity to O1 Vibrio cholerae, there are limitations in this assay to detect instances of reexposure. We define the conditions operative in producing secondary vibriocidal responses in North American volunteers primed with either wild-type V. cholerae 1, 4, or 6 months later. Secondary serum vibriocidal responses occurred under two distinct secondary challenge conditions. The first occurred when secondary challenge produced a breakthrough in clinical protection. Following secondary exposure, 14 of 22 (64%) and 1 of 29 (3%) subjects with and without vibrio stool excretion, respectively, had secondary responses (P < 0.001); 5 of 6 (83%) and 10 of 45 (22%) subjects with or without diarrhea, respectively, mounted a secondary response (P = 0.006). The second condition occurred in the presence of full clinical protection but was dependent on the time interval between exposure. No subject (0 to 17) vaccinated with CVD 103-HgR and given homologous wild-type challenge within 4 months mounted a secondary vibriocidal response (P = 0.0009). The majority of the serum vibriocidal activity was of the immunoglobulin M (IgM) isotype, seen in 96 and 73% of subjects following primary and secondary exposure, respectively. Vibriocidal activity in the IgG fraction following primary and secondary exposures occurred with < or = 50% of volunteers; lipopolysaccharide (LPS)-specific IgG1 and IgG3 subclass responses supported the vibriocidal isotype data. However, following primary exposure, IgG4 LPS responses predominated, occurring in 81% of responding volunteers. These data suggest that, under certain conditions of secondary exposure to V. cholerae O1 antigens, when there is sufficient active local immunity present, there is a block of vibrio antigen resampling at the M cell level. We discuss the implications of and possible explanations for these findings.
机译:尽管血清杀线虫活性被广泛用作抗O1霍乱弧菌的免疫标志物,但该检测方法在检测再暴露情况方面存在局限性。我们定义了在野生型霍乱弧菌感染1、4或6个月后引发的北美志愿者中产生次级杀线虫反应的有效条件。在两个不同的次级激发条件下发生了次级血清杀线虫反应。第一次发生在继发性攻击在临床保护方面取得突破的时候。继发暴露后,有或没有弧菌性粪便排泄的22名受试者中有14名(64%)和29名受试者中有1名(3%)发生了继发性反应(P <0.001)。有腹泻或无腹泻的6名受试者中有5名(83%)和45名受试者中有10名(22%)发生了次要反应(P = 0.006)。第二种情况在完全临床保护的情况下发生,但取决于暴露之间的时间间隔。没有受试者(0至17岁)接种了CVD 103-HgR疫苗并在4个月内接受了同源野生型攻击,没有发生继发杀线虫反应(P = 0.0009)。大部分的血清杀病毒活性是免疫球蛋白M(IgM)同种型,分别在初次和二次暴露后分别在96%和73%的受试者中观察到。 ≤50%的志愿者在初次和二次接触后IgG组分中具有杀线活性。脂多糖(LPS)特异性IgG1和IgG3亚类响应支持杀线虫同种型数据。然而,在初次接触后,IgG4 LPS反应占主导地位,发生在81%的反应志愿者中。这些数据表明,在二次暴露于霍乱弧菌O1抗原的某些条件下,当存在足够的活动局部免疫力时,在M细胞水平上会有一个弧菌抗原重采样区。我们讨论这些发现的含义和可能的解释。

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