Literature DB >> 1580685

T cell immunodeficiency in dyskeratosis congenita.

B W Lee1, H K Yap, T C Quah, A Chong, C C Seah.   

Abstract

Dyskeratosis congenita has been found to be associated with abnormal immune function. In this study we report a patient with this association. He developed Pneumocystis carinii interstitial pneumonia, and impaired cell mediated immunity was confirmed by the presence of depressed lymphoproliferative responses to in vitro stimulation with mitogen. Enumeration of T cell subsets showed a severely depressed CD4:CD8 ratio (0.38), which is the likely cause for impaired cell mediated immunity. The T cell activation pathway appeared intact, as his T lymphocytes were able to express activation markers (CD25 and HLA-DR) after mitogen stimulation.

Entities:  

Mesh:

Year:  1992        PMID: 1580685      PMCID: PMC1793336          DOI: 10.1136/adc.67.4.524

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  14 in total

1.  Primary immunodeficiency diseases. Report of a World Health Organization scientific group.

Authors: 
Journal:  Clin Immunol Immunopathol       Date:  1986-07

2.  Congenital dyskeratosis and immunological defect.

Authors:  C Borrone; F Dagna Bricarelli; C Astrice; P Moscatelli
Journal:  Boll Ist Sieroter Milan       Date:  1974

3.  Two cases of dyskeratosis congenita presenting with aplastic anemia.

Authors:  B W Lee; H K Yap; H B Wong; Y C Giam
Journal:  J Singapore Paediatr Soc       Date:  1982

4.  Dyskeratosis congenita: relationship to Fanconi's anemia.

Authors:  W Steier; G A Van Voolen; V J Selmanowitz
Journal:  Blood       Date:  1972-04       Impact factor: 22.113

5.  Assignment of the gene for dyskeratosis congenita to Xq28.

Authors:  J M Connor; D Gatherer; F C Gray; L A Pirrit; N A Affara
Journal:  Hum Genet       Date:  1986-04       Impact factor: 4.132

6.  X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.

Authors:  J M Puck; R L Nussbaum; D L Smead; M E Conley
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

7.  Enhanced G2 chromatid radiosensitivity in dyskeratosis congenita fibroblasts.

Authors:  D M DeBauche; G S Pai; W S Stanley
Journal:  Am J Hum Genet       Date:  1990-02       Impact factor: 11.025

8.  X-linked dyskeratosis congenita with pancytopenia.

Authors:  A Gutman; A Frumkin; A Adam; N Bloch-Shtacher; L A Rozenszajn
Journal:  Arch Dermatol       Date:  1978-11

9.  Defective humoral immunity in pediatric acquired immune deficiency syndrome.

Authors:  L J Bernstein; H D Ochs; R J Wedgwood; A Rubinstein
Journal:  J Pediatr       Date:  1985-09       Impact factor: 4.406

10.  Cellular and genetic analyses of IL-2 production and IL-2 receptor expression in a patient with familial T-cell-dominant immunodeficiency.

Authors:  S Doi; O Saiki; T Tanaka; K Ha-Kawa; T Igarashi; T Fujita; T Taniguchi; S Kishimoto
Journal:  Clin Immunol Immunopathol       Date:  1988-01
View more
  6 in total

1.  Telomere Length and Use of Immunosuppressive Medications in Idiopathic Pulmonary Fibrosis.

Authors:  Chad A Newton; David Zhang; Justin M Oldham; Julia Kozlitina; Shwu-Fan Ma; Fernando J Martinez; Ganesh Raghu; Imre Noth; Christine Kim Garcia
Journal:  Am J Respir Crit Care Med       Date:  2019-08-01       Impact factor: 21.405

2.  Immune status of patients with inherited bone marrow failure syndromes.

Authors:  Neelam Giri; Blanche P Alter; Keri Penrose; Roni T Falk; Yuanji Pan; Sharon A Savage; Marcus Williams; Troy J Kemp; Ligia A Pinto
Journal:  Am J Hematol       Date:  2015-05-28       Impact factor: 10.047

3.  Treatment of the hematological manifestations of dyskeratosis congenita.

Authors:  C Putterman; R Safadi; J Zlotogora; R Banura; A Eldor
Journal:  Ann Hematol       Date:  1993-04       Impact factor: 3.673

4.  Short telomeres are sufficient to cause the degenerative defects associated with aging.

Authors:  Mary Armanios; Jonathan K Alder; Erin M Parry; Baktiar Karim; Margaret A Strong; Carol W Greider
Journal:  Am J Hum Genet       Date:  2009-12       Impact factor: 11.025

Review 5.  The telomere syndromes.

Authors:  Mary Armanios; Elizabeth H Blackburn
Journal:  Nat Rev Genet       Date:  2012-09-11       Impact factor: 53.242

Review 6.  FOXN1 deficient nude severe combined immunodeficiency.

Authors:  Ioanna A Rota; Fatima Dhalla
Journal:  Orphanet J Rare Dis       Date:  2017-01-11       Impact factor: 4.123

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.