首页> 美国卫生研究院文献>Infection and Immunity >Serum opsonic activity after immunization of adults with Haemophilus influenzae type b-diphtheria toxoid conjugate vaccine.
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Serum opsonic activity after immunization of adults with Haemophilus influenzae type b-diphtheria toxoid conjugate vaccine.

机译:用流感嗜血杆菌b型白喉类毒素结合疫苗免疫成人后的血清调理活性。

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摘要

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.
机译:我们测量了人类多形核白细胞对放射性标记的b型流感嗜血杆菌的摄取。从六名接受b型多糖疫苗(PRP)免疫的成年人或六名接受与白喉类毒素共价偶联的PRP免疫的成年人(PRP-D疫苗)的血清中分别对b型流感嗜血杆菌菌株进行了调理作用。使用前将血清热灭活,并添加外源人补体。在12名受试者中,有3名在其免疫前血清中具有高水平的调理活性(大于免疫控制的40%)。该活性与抗PRP抗体的浓度不相关,并且不受抗PRP抗体吸收的影响。接种疫苗后1个月,PRP-D受试者的血清调理活性高于接受PRP的受试者(5%血清,平均PRP-D = 86%,平均PRP = 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),但两组之间没有差异(平均PRP-D = 48%,平均PRP = 51%)。在免疫后血清中,由PRP-D或PRP疫苗诱导的调理活性与通过放射抗原结合测定法测得的抗PRP抗体浓度直接相关。我们得出的结论是,两种疫苗均能诱导调理活性,成人免疫所诱导的调理活性与所获得的抗PRP抗体浓度密切相关,并且在具有低浓度抗PRP抗体的免疫前血清中,除抗PRP抗体外的其他因素也有助于调理活动。

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