Adult-onset immunodeficiency in Thailand and Taiwan.

نویسندگان

  • Sarah K Browne
  • Peter D Burbelo
  • Ploenchan Chetchotisakd
  • Yupin Suputtamongkol
  • Sasisopin Kiertiburanakul
  • Pamela A Shaw
  • Jennifer L Kirk
  • Kamonwan Jutivorakool
  • Rifat Zaman
  • Li Ding
  • Amy P Hsu
  • Smita Y Patel
  • Kenneth N Olivier
  • Viraphong Lulitanond
  • Piroon Mootsikapun
  • Siriluck Anunnatsiri
  • Nasikarn Angkasekwinai
  • Boonmee Sathapatayavongs
  • Po-Ren Hsueh
  • Chi-Chang Shieh
  • Margaret R Brown
  • Wanna Thongnoppakhun
  • Reginald Claypool
  • Elizabeth P Sampaio
  • Charin Thepthai
  • Duangdao Waywa
  • Camilla Dacombe
  • Yona Reizes
  • Adrian M Zelazny
  • Paul Saleeb
  • Lindsey B Rosen
  • Allen Mo
  • Michael Iadarola
  • Steven M Holland
چکیده

BACKGROUND Autoantibodies against interferon-γ are associated with severe disseminated opportunistic infection, but their importance and prevalence are unknown. METHODS We enrolled 203 persons from sites in Thailand and Taiwan in five groups: 52 patients with disseminated, rapidly or slowly growing, nontuberculous mycobacterial infection (group 1); 45 patients with another opportunistic infection, with or without nontuberculous mycobacterial infection (group 2); 9 patients with disseminated tuberculosis (group 3); 49 patients with pulmonary tuberculosis (group 4); and 48 healthy controls (group 5). Clinical histories were recorded, and blood specimens were obtained. RESULTS Patients in groups 1 and 2 had CD4+ T-lymphocyte counts that were similar to those in patients in groups 4 and 5, and they were not infected with the human immunodeficiency virus (HIV). Washed cells obtained from patients in groups 1 and 2 had intact cytokine production and a response to cytokine stimulation. In contrast, plasma obtained from these patients inhibited the activity of interferon-γ in normal cells. High-titer anti-interferon-γ autoantibodies were detected in 81% of patients in group 1, 96% of patients in group 2, 11% of patients in group 3, 2% of patients in group 4, and 2% of controls (group 5). Forty other anticytokine autoantibodies were assayed. One patient with cryptococcal meningitis had autoantibodies only against granulocyte-macrophage colony-stimulating factor. No other anticytokine autoantibodies or genetic defects correlated with infections. There was no familial clustering. CONCLUSIONS Neutralizing anti-interferon-γ autoantibodies were detected in 88% of Asian adults with multiple opportunistic infections and were associated with an adult-onset immunodeficiency akin to that of advanced HIV infection. (Funded by the National Institute of Allergy and Infectious Diseases and the National Institute of Dental and Craniofacial Research; ClinicalTrials.gov number, NCT00814827.).

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عنوان ژورنال:
  • The New England journal of medicine

دوره 367 8  شماره 

صفحات  -

تاریخ انتشار 2012