Morra Massimo, Barrington Robert A, Abadia-Molina Ana C, Okamoto Susumo, Julien Aimee, Gullo Charles, Kalsy Anuj, Edwards Matthew J, Chen Gang, Spolski Rosanne, Leonard Warren J, Huber Brigitte T, Borrow Persephone, Biron Christine A, Satoskar Abhay R, Carroll Michael C, Terhorst Cox
Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Proc Natl Acad Sci U S A. 2005 Mar 29;102(13):4819-23. doi: 10.1073/pnas.0408681102. Epub 2005 Mar 17.
More than half of patients with X-linked lympho-proliferative disease, which is caused by a defect in the intracellular adapter protein SH2D1A, suffer from an extreme susceptibility to Epstein-Barr virus. One-third of these patients, however, develop dysgammaglobulenemia without an episode of severe mononucleosis. Here we show that in SH2D1A(-/-) mice, both primary and secondary responses of all Ig subclasses are severely impaired in response to specific antigens. Because germinal centers were absent in SH2D1A(-/-) mice upon primary immunization, and because SH2D1A was detectable in wt germinal center B cells, we examined whether SH2D1A(-/-) B cell functions were impaired. Using the adoptive cotransfer of B lymphocytes from hapten-primed SH2D1A(-/-) mice with CD4(+) T cells from primed wt mice into irradiated wt mice provided evidence that signal transduction events controlled by SH2D1A are essential for B cell activities resulting in antigen specific IgG production. Defects in naive SH2D1A(-/-) B cells became evident upon cotransfer with non-primed wt CD4(+) cells into Rag2(-/-) recipients. Thus, both defective T and B cells exist in the absence of SH2D1A, which may explain the progressive dysgammaglobulinemia in a subset of X-linked lympho-proliferative disease patients without involvement of Epstein-Barr virus.
超过半数由细胞内衔接蛋白SH2D1A缺陷引起的X连锁淋巴增殖性疾病患者对爱泼斯坦-巴尔病毒极度易感。然而,这些患者中有三分之一会发生γ球蛋白异常血症,却没有严重单核细胞增多症发作。我们在此表明,在SH2D1A基因敲除小鼠中,所有Ig亚类对特定抗原的初次和二次反应均严重受损。由于初次免疫后SH2D1A基因敲除小鼠中没有生发中心,且在野生型生发中心B细胞中可检测到SH2D1A,我们研究了SH2D1A基因敲除的B细胞功能是否受损。将经半抗原致敏的SH2D1A基因敲除小鼠的B淋巴细胞与经致敏的野生型小鼠的CD4(+) T细胞过继共转移到经辐照的野生型小鼠中,这提供了证据,表明由SH2D1A控制的信号转导事件对于导致抗原特异性IgG产生的B细胞活动至关重要。当与未致敏的野生型CD4(+) 细胞共转移到Rag2基因敲除受体中时,幼稚的SH2D1A基因敲除B细胞中的缺陷变得明显。因此,在没有SH2D1A的情况下存在有缺陷的T细胞和B细胞,这可能解释了一部分未感染爱泼斯坦-巴尔病毒的X连锁淋巴增殖性疾病患者中进行性γ球蛋白异常血症的原因。