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两名患有免疫缺陷和早发性全身性皮炎的婴儿胸腺输出受损及T细胞库受限。

Impaired thymic output and restricted T-cell repertoire in two infants with immunodeficiency and early-onset generalized dermatitis.

作者信息

Pirovano S, Mazzolari E, Pasic S, Albertini A, Notarangelo Luigi D, Imberti L

机构信息

Terzo Servizio Analisi, Spedali Civili of Brescia, Brescia, Italy.

出版信息

Immunol Lett. 2003 Mar 3;86(1):93-7. doi: 10.1016/s0165-2478(02)00291-2.

Abstract

We evaluated the T-cell repertoire and the thymic output in two infants, one with Omenn Syndrome (OS) and another with complete DiGeorge Syndrome (DGS), who developed generalized dermatitis. The patients shared common T-cell abnormalities, as demonstrated by the low response to mitogenic stimulation, by an unusual usage of specific T-cell receptor (TCR) segments, and by a reduction of TCR diversity in both alpha/beta and gamma/delta populations. Furthermore, they both showed an impaired thymic function, as assessed by the low number of TCR recombination excision circles, which are formed from excised DNA during the rearrangement of TCR genes. These data indicated that generalized erythrodermia may be present in different forms of T-cell immunodeficiency and may reflect intrinsic defects in either V(D)J recombination or in thymic development, leading to the peripheral expansion of T-cell clonotypes, that bear peculiar TCR chains.

摘要

我们评估了两名患有全身性皮炎的婴儿的T细胞库和胸腺输出,其中一名患有奥门综合征(OS),另一名患有完全性22q11.2缺失综合征(DGS)。这两名患者具有共同的T细胞异常,表现为对丝裂原刺激反应低下、特定T细胞受体(TCR)片段的异常使用,以及α/β和γ/δ群体中TCR多样性的降低。此外,通过TCR重组切除环数量减少评估,他们的胸腺功能均受损,TCR重组切除环是在TCR基因重排过程中由切除的DNA形成的。这些数据表明,全身性红皮病可能存在于不同形式的T细胞免疫缺陷中,并且可能反映V(D)J重组或胸腺发育中的内在缺陷,导致携带特殊TCR链的T细胞克隆型在外周扩增。

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