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成人接种b型流感嗜血杆菌-白喉类毒素结合疫苗后的血清调理活性。

Serum opsonic activity after immunization of adults with Haemophilus influenzae type b-diphtheria toxoid conjugate vaccine.

作者信息

Cates K L, Marsh K H, Granoff D M

出版信息

Infect Immun. 1985 Apr;48(1):183-9. doi: 10.1128/iai.48.1.183-189.1985.

DOI:10.1128/iai.48.1.183-189.1985
PMID:3872263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC261933/
Abstract

We measured the uptake of radiolabeled Haemophilus influenzae type b by human polymorphonuclear leukocytes. Haemophilus influenzae type b strains were preopsonized in individual sera from six adults immunized with type b polysaccharide vaccine (PRP) or six adults immunized with PRP covalently coupled to diphtheria toxoid (PRP-D vaccine). Serum was heat inactivated before use, and exogenous human complement was added. Of the 12 subjects, 3 had high levels of opsonic activity (greater than 40% of immune control) in their preimmunization serum. This activity did not correlate with the concentrations of anti-PRP antibody and was unaffected by absorption of anti-PRP antibody. At 1 month after vaccination, the serum of PRP-D subjects had higher opsonic activity than that from subjects who received PRP (5% serum, mean PRP-D = 86%, mean PRP = 53%, P = 0.001). After 12 months, both groups had higher serum opsonic activity than before immunization (P less than 0.02), but there was no difference between the two groups (mean PRP-D = 48%, mean PRP = 51%). In postimmunization serum, opsonic activity induced by PRP-D or PRP vaccines correlated directly with anti-PRP antibody concentrations as measured by a radioantigen binding assay. We conclude that both vaccines induce opsonic activity, opsonic activity induced by immunization of adults correlates well with the concentration of anti-PRP antibody achieved, and in preimmune sera with low concentrations of anti-PRP antibody, factors other than anti-PRP antibody contribute to opsonic activity.

摘要

我们检测了人多形核白细胞对放射性标记的b型流感嗜血杆菌的摄取情况。b型流感嗜血杆菌菌株在来自6名接种b型多糖疫苗(PRP)的成年人或6名接种与白喉类毒素共价偶联的PRP(PRP-D疫苗)的成年人的个体血清中进行预调理。血清在使用前进行热灭活,并添加外源性人补体。在这12名受试者中,3人在免疫前血清中具有高水平的调理活性(大于免疫对照的40%)。这种活性与抗PRP抗体的浓度无关,并且不受抗PRP抗体吸收的影响。接种疫苗1个月后,PRP-D受试者的血清调理活性高于接受PRP的受试者(5%血清,PRP-D平均为86%,PRP平均为53%,P = 0.001)。12个月后,两组的血清调理活性均高于免疫前(P小于0.02),但两组之间无差异(PRP-D平均为48%,PRP平均为51%)。在免疫后血清中,PRP-D或PRP疫苗诱导的调理活性与通过放射抗原结合试验测量的抗PRP抗体浓度直接相关。我们得出结论,两种疫苗均诱导调理活性,成人免疫诱导的调理活性与所达到的抗PRP抗体浓度密切相关,并且在抗PRP抗体浓度低的免疫前血清中,除抗PRP抗体外的其他因素也有助于调理活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c02/261933/93dceff7c830/iai00115-0194-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c02/261933/93dceff7c830/iai00115-0194-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c02/261933/93dceff7c830/iai00115-0194-a.jpg

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