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年轻男性中针对爱泼斯坦-巴尔病毒决定抗原的细胞免疫缺陷

Cellular immune defects to Epstein-Barr virus-determined antigens in young males.

作者信息

Masucci M G, Szigeti R, Ernberg I, Masucci G, Klein G, Chessels J, Sieff C, Lie S, Glomstein A, Businco L, Henle W, Henle G, Pearson G, Sakamoto K, Purtilo D T

出版信息

Cancer Res. 1981 Nov;41(11 Pt 1):4284-91.

PMID:6171337
Abstract

Three males with the X-linked lymphoproliferative syndrome (XLP) with hypo- or agammaglobulinemia following Epstein-Barr virus (EBV) infection and two males with the chronic mononucleosis syndrome were investigated for immune responses to EBV-determined antigens. Males with XLP showed profound cellular immune defects. Markedly diminished responses of natural killer cell and interferon-activated killer cell activities and impaired leukocyte migration inhibition responses to phytohemagglutinin were determined in patients with XLP. The two patients with chronic mononucleosis showed less severe defects. All patients showed partial or complete impairment of their EBV-specific immune responses as measured by leukocyte migration inhibition. EBV-specific antibodies were markedly diminished against EBV-associated nuclear antigen, early antigen, and viral capsid antigen in males with XLP. In contrast, patients with chronic mononucleosis had elevated antibodies to most EBV-specific antigens. Individuals with life-threatening EBV-induced lymphoproliferative disorders may exhibit multiple defective immune mechanisms against the virus.

摘要

对3名患有X连锁淋巴细胞增生综合征(XLP)且在感染爱泼斯坦-巴尔病毒(EBV)后出现低丙种球蛋白血症或无丙种球蛋白血症的男性以及2名患有慢性单核细胞增多症综合征的男性进行了针对EBV决定抗原的免疫反应研究。患有XLP的男性表现出严重的细胞免疫缺陷。在XLP患者中,自然杀伤细胞和干扰素激活杀伤细胞活性的反应明显减弱,对植物血凝素的白细胞迁移抑制反应受损。两名患有慢性单核细胞增多症的患者表现出的缺陷较轻。通过白细胞迁移抑制测定,所有患者的EBV特异性免疫反应均部分或完全受损。患有XLP的男性针对EBV相关核抗原、早期抗原和病毒衣壳抗原的EBV特异性抗体明显减少。相比之下,患有慢性单核细胞增多症的患者针对大多数EBV特异性抗原的抗体升高。患有危及生命的EBV诱导淋巴细胞增生性疾病的个体可能表现出针对该病毒的多种缺陷免疫机制。

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