HIV感染者对破伤风类毒素和肺炎球菌荚膜多糖抗体反应的时间过程。

E Talesnik, P A Vial, J Labarca, C Méndez, X Soza
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引用次数: 23

摘要

评估了hiv感染患者对t细胞依赖性和t细胞非依赖性2型抗原的体液免疫反应的时间过程。共有26例血清阳性患者接种了破伤风类毒素和23价肺炎球菌疫苗;接种后基线、接种后2个月和12个月分别检测破伤风类毒素(Ttox)总IgG和IgG1抗体以及23种肺炎链球菌荚膜抗原(PPS)总IgG和IgG2抗体。对于Ttox,在刺激后2个月,IgG1 (Ttox-IgG1)的基线水平从11.0 mg/L增加到19.5 mg/L。总的来说,只有6名患者(23%)表现出显著的反应。在疫苗接种后12个月,Ttox-IgG和T-tox-IgG1显著低于基线水平(Ttox IgG基础;11.0 mg/L, 12个月;0.8 mg/L, Ttox IgG1基线;13.1 mg/L, Ttox IgG1 12个月;2.4 mg/L), 10名患者的抗体低于保护水平(0.6 mg/L)。与PPS相比,在第2个月和第12个月观察到显著的应答(PPS- igg基础;35.9 U/ml, 2个月;151.4 U/ml, 12个月;59.7 U /毫升;PPS-IgG2基线20.3 U/ml, 2个月;113.2 U/ml, 12个月;51.9 U /毫升)。总体而言,19例患者(76%)对肺炎球菌多糖抗原表现出免疫应答。使用Ttox t细胞依赖抗原免疫不能引起显著的免疫应答,并可能导致hiv感染患者的抗体产生抑制。相比之下,使用t细胞非依赖性2型抗原进行免疫接种可使肺炎球菌多糖在很大比例的hiv感染患者中诱导显著的免疫应答。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time course of antibody response to tetanus toxoid and pneumococcal capsular polysaccharides in patients infected with HIV.

The temporal course of the humoral immune response to T-cell-dependent and T-cell-independent type 2 antigens was evaluated in HIV-infected patients. In all, 26 seropositive patients were vaccinated with tetanus toxoid and 23-valent pneumococcal vaccines; total IgG and IgG1 antibodies to tetanus toxoid (Ttox) and total IgG and IgG2 antibodies against 23 Streptococcus pneumoniae capsular antigens (PPS) were measured at baseline, 2 months, and 12 months after vaccination. For the Ttox, baseline levels of IgG1 (Ttox-IgG1) increased from 11.0 to 19.5 mg/L at 2 months postimmunization. Overall only 6 patients (23%) showed a significant response. At 12 months postvaccination, Ttox-IgG and T-tox-IgG1 were significantly lower than baseline levels (Ttox IgG basal; 11.0 mg/L, 12 months; 0.8 mg/L, Ttox IgG1 baseline; 13.1 mg/L, Ttox IgG1 12 months; 2.4 mg/L) and in 10 patients, antibodies that fell below protective levels (0.6 mg/L). In contrast with PPS, a significant response was observed at 2 and 12 months (PPS-IgG basal; 35.9 U/ml, 2 months; 151.4 U/ml, 12 months; 59.7 U/ml; PPS-IgG2 baseline 20.3 U/ml, 2 months; 113.2 U/ml, 12 months; 51.9 U/ml). Overall, 19 patients (76%) showed an immune response to pneumococcal polysaccharides antigens. Immunization with the Ttox T-cell-dependent antigen fails to elicit a significant immune response and may induce inhibition of antibody production in HIV-infected patients. In contrast, immunization with a T-cell-independent type 2 antigen can cause the pneumococcal polysaccharides to induce significant immune response in a high proportion of HIV-infected patients.

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