T-cell immunodeficiencies

被引：19

作者：

Elder, ME ^{[1
]}

机构：

[1] Univ Calif San Francisco, Dept Pediat, Div Pediat Immunol Allergy Rheumatol, San Francisco, CA 94143 USA

来源：

PEDIATRIC CLINICS OF NORTH AMERICA | 2000年 / 47卷 / 06期

关键词：

D O I：

10.1016/S0031-3955(05)70270-4

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Inherited defects in T-cell function result in severe combined immunodeficiency, combined T- and B-cell defects, and disorders that selectively involve cellular immune responses. The clinical, laboratory, and molecular features of primary T-cell immune deficiencies are discussed.

引用

页码：1253 / +

页数：23

共 68 条

[51] The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM [J].

Sayos, J ;

Wu, C ;

Morra, M ;

Wang, N ;

Zhang, X ;

Allen, D ;

van Schaik, S ;

Notarangelo, L ;

Geha, R ;

Roncarolo, MG ;

Oettgen, H ;

De Vries, JE ;

Aversa, G ;

Terhorst, C .

NATURE, 1998, 395 (6701) :462-469

[52] Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2) [J].

Schuffenhauer, S ;

Lichtner, P ;

Peykar-Derakhshandeh, P ;

Murken, J ;

Haas, OA ;

Back, E ;

Wolff, G ;

Zabel, B ;

Barisic, I ;

Rauch, A ;

Borochowitz, Z ;

Dallapiccola, B ;

Ross, M ;

Meitinger, T .

EUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 (03) :213-225

[53]

Schuster V, 1999, PRIMARY IMMUNODEFICIENCY DISEASES, P222

[54] RAG mutations in human B cell-negative SCID [J].

Schwarz, K ;

Gauss, GH ;

Ludwig, L ;

Pannicke, U ;

Li, Z ;

Lindner, D ;

Friedrich, W ;

Seger, RA ;

HansenHagge, TE ;

Desiderio, S ;

Lieber, MR ;

Bartram, CR .

SCIENCE, 1996, 274 (5284) :97-99

[55]

Schwarz K, 1999, PRIMARY IMMUNODEFICIENCY DISEASES, P155

[56]

Seidemann K, 1999, MED PEDIATR ONCOL, V33, P536, DOI 10.1002/(SICI)1096-911X(199912)33:6<536::AID-MPO3>3.0.CO

[57]

2-Z

[58] The Wiskott-Aldrich syndrome protein (WASP): Roles in signaling and cytoskeletal organization [J].

Snapper, SB ;

Rosen, FS .

ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :905-929

[59] SEVERE COMBINED IMMUNODEFICIENCY - A RETROSPECTIVE SINGLE-CENTER STUDY OF CLINICAL PRESENTATION AND OUTCOME IN 117 PATIENTS [J].

STEPHAN, JL ;

VLEKOVA, V ;

LEDEIST, F ;

BLANCHE, S ;

DONADIEU, J ;

DESAINTBASILE, G ;

DURANDY, A ;

GRISCELLI, C ;

FISCHER, A .

JOURNAL OF PEDIATRICS, 1993, 123 (04) :564-572

[60] Lack of correlation between impaired T cell production, immunodeficiency, and other phenotypic features in chromosome 22q11.2 deletion syndromes (DiGeorge Syndrome Velocardiofacial syndrome) [J].

Sullivan, KE ;

Jawad, AF ;

Randall, P ;

Driscoll, DA ;

Emanuel, BS ;

McDonald-McGinn, DM ;

Zackai, EH .

CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 86 (02) :141-146

← 1 2 3 4 5 6 7 →