Dichotomy between T Cell and B Cell Tolerance to Neonatal Retroviral Infection Permits T Cell Therapy

Bettina Mavrommatis, L. Baudino, Prisca Lévy, Julia Merkenschlager, U. Eksmond, T. Donnarumma, G. Young, J. Stoye, G. Kassiotis
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引用次数: 1

Abstract

Elucidation of the immune requirements for control or elimination of retroviral infection remains an important aim. We studied the induction of adaptive immunity to neonatal infection with a murine retrovirus, under conditions leading to immunological tolerance. We found that the absence of either maternal or offspring adaptive immunity permitted efficient vertical transmission of the retrovirus. Maternal immunodeficiency allowed the retrovirus to induce central Th cell tolerance in the infected offspring. In turn, this compromised the offspring’s ability to mount a protective Th cell–dependent B cell response. However, in contrast to T cells, offspring B cells were not centrally tolerized and retained their ability to respond to the infection when provided with T cell help. Thus, escape of retrovirus-specific B cells from deletional tolerance offers the opportunity to induce protective retroviral immunity by restoration of retrovirus-specific T cell help, suggesting similar T cell immunotherapies for persistent viral infections.
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T细胞和B细胞对新生儿逆转录病毒感染耐受的二分法允许T细胞治疗
阐明控制或消除逆转录病毒感染的免疫需求仍然是一个重要目标。我们研究了在导致免疫耐受的条件下,小鼠逆转录病毒对新生儿感染的适应性免疫诱导。我们发现,缺乏母体或后代的适应性免疫允许逆转录病毒有效的垂直传播。母体免疫缺陷使逆转录病毒在受感染的后代中诱导中央Th细胞耐受。反过来,这损害了后代建立依赖于Th细胞的保护性B细胞反应的能力。然而,与T细胞相反,子代B细胞在T细胞的帮助下不具有中央耐受性,并保留了对感染的反应能力。因此,逆转录病毒特异性B细胞从缺失耐受中逃脱,为通过恢复逆转录病毒特异性T细胞帮助诱导保护性逆转录病毒免疫提供了机会,这表明类似的T细胞免疫疗法可用于持续性病毒感染。
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