| Literature DB >> 19621458 |
Kawsar R Talaat1, Jennifer A Rothman, Jeffrey I Cohen, Mariarita Santi, John K Choi, Miguel Guzman, Robert Zimmerman, Sudha Nallasamy, Alexander Brucker, Martha Quezado, Stefania Pittaluga, Nicholas J Patronas, Amy D Klion, Kim E Nichols.
Abstract
X-linked lymphoproliferative disease (XLP) is an immunodeficiency caused by defects in the adaptor molecule SAP. The manifestations of XLP generally occur following Epstein-Barr virus (EBV) infection and include fulminant mononucleosis, hypogammaglobulinemia and lymphoma. In this report, we describe two unrelated patients with fatal T-cell-mediated central nervous system vasculitis for whom repeated serologic and molecular testing for EBV was negative. In both patients, clonal T-cell populations were observed, but neither demonstrated evidence of lymphoma. Thus, loss of SAP function can lead to dysregulated immune responses characterized by the uncontrolled expansion and activation of T cells independent of EBV infection.Entities:
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Year: 2009 PMID: 19621458 PMCID: PMC2745493 DOI: 10.1002/pbc.22185
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167