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用热灭活麻风杆菌对人类志愿者进行疫苗接种:与麻风菌素反应解读相关的局部反应

Vaccination of human volunteers with heat-killed M. leprae: local responses in relation to the interpretation of the lepromin reaction.

作者信息

Gill H K, Mustafa A S, Godal T

机构信息

Department of Pathology, Norwegian Radium Hospital, Oslo.

出版信息

Int J Lepr Other Mycobact Dis. 1988 Mar;56(1):36-44.

PMID:3286799
Abstract

The early (Fernandez) and late (Mitsuda) lepromin reactions were closely examined in a group of healthy, BCG-vaccinated individuals who were given four doses of a heat-killed, armadillo-derived vaccine, i.e., 1.5 X 10(7), 5 X 10(7), 1.5 X 10(8), and 5 X 10(8) bacilli. There was a clear dose-response relationship for both the early and late reactions with no leveling of the responses within the range of doses examined. While the early response was negative in most of the volunteers, the late response was positive in all of the volunteers. No association was found between the early lepromin test and the pre-vaccination skin test to PPD. There was also no association between the early lepromin test and the pre-vaccination skin test response to a soluble Mycobacterium leprae antigenic preparation (MLSA) in general, but there was a good correlation between these two parameters at the highest vaccine dose. The late lepromin response showed no association with either the prevaccination or post-vaccination skin test response to PPD. However, there was a significant correlation between the late lepromin response and the post-vaccination skin test response to MLSA. In general, no association could be found between the in vivo skin tests and the in vitro lymphocyte transformation test (LTT). Thus, the lepromin test is essentially a vaccination which elicits a specific response to M. leprae antigens provided that the dose of armadillo lepromin given is higher than 5 X 10(7). Therefore, it is unsuitable as a diagnostic test for leprosy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对一组接种卡介苗的健康个体进行了密切观察,这些个体接种了四剂经热灭活的犰狳源疫苗,即1.5×10⁷、5×10⁷、1.5×10⁸和5×10⁸条杆菌,以观察早期(费尔南德斯)和晚期(光田)麻风菌素反应。早期和晚期反应均存在明显的剂量反应关系,在所检测的剂量范围内反应没有趋于平稳。虽然大多数志愿者的早期反应为阴性,但所有志愿者的晚期反应均为阳性。未发现早期麻风菌素试验与接种前PPD皮肤试验之间存在关联。总体而言,早期麻风菌素试验与接种前对可溶性麻风分枝杆菌抗原制剂(MLSA)的皮肤试验反应之间也没有关联,但在最高疫苗剂量下,这两个参数之间存在良好的相关性。晚期麻风菌素反应与接种前或接种后PPD皮肤试验反应均无关联。然而,晚期麻风菌素反应与接种后对MLSA的皮肤试验反应之间存在显著相关性。一般来说,体内皮肤试验与体外淋巴细胞转化试验(LTT)之间未发现关联。因此,麻风菌素试验本质上是一种疫苗接种,只要给予的犰狳麻风菌素剂量高于5×10⁷,就会引发对麻风分枝杆菌抗原的特异性反应。所以,它不适用于麻风病的诊断试验。(摘要截短于250字)

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