Literature DB >> 12114290

Immunological responses are not abnormal in symptomatic Gulf War veterans.

Michael P Everson1, Ke Shi, Peggy Aldridge, Alfred A Bartolucci, Warren D Blackburn.   

Abstract

The underlying etiology and pathogenesis of Gulf War veterans' illnesses continue to be under intense investigation. Reports have suggested the basis for these illnesses may be an altered immune system, but compelling evidence is lacking. We sought to determine whether in vitro immune responses were abnormal in symptomatic Gulf War veterans relative to matched controls. A randomized case-control study was conducted by blinded comparison of laboratory measures of in vitro immune responses in blood samples obtained from veterans in an outpatient facility of a Veterans Affairs medical center. Symptomatic Gulf War veterans with otherwise undefined illnesses (52 symptomatic subjects), asymptomatic Gulf War veterans (31 asymptomatic controls), and veterans who had applied for disability compensation and had not participated in the Gulf War (21 disability controls) represented the volunteer sample. In vitro cellular and humoral immune responses were measured to detect functional abnormalities in antigen presenting cells (autologous mixed leukocyte reactions and expression of interleukin (IL)-1beta, IL-6, IL-10, and tumor necrosis factor-alpha); T cells (lymphocyte proliferation using the polyclonal T-cell activators phytohemagglutinin and Concanavalin A; primary immune responses in allogeneic mixed leukocyte reactions; secondary immune response using the recall antigens tetanus toxoid, Candida albicans, and anthrax vaccine; and soluble IL-2 receptor expression); type-1 T-helper cells (gamma interferon expression); type-2 T-helper cells (IL-4 and IL-10 expression); and B cells (polyclonal B-cell activator pokeweed mitogen-induced immunoglobulin production). In general, immune response measures did not differ significantly between groups. Heightened responses observed in the disability control group (sporadically greater responses to one mitogen and two antigens) and the Gulf War participation control group (greater recall responses to anthrax vaccine) did not suggest impaired immune cell function in symptomatic veterans when compared with controls. We conclude that in vitro immunological responses are not abnormal in symptomatic Gulf War veterans.

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Year:  2002        PMID: 12114290     DOI: 10.1111/j.1749-6632.2002.tb04233.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  6 in total

1.  Cellular immune activation in Gulf War veterans.

Authors:  Anna Skowera; Matthew Hotopf; Elzbieta Sawicka; Ruben Varela-Calvino; Catherine Unwin; Vasilis Nikolaou; Lisa Hull; Khalida Ismail; Anthony S David; Simon C Wessely; Mark Peakman
Journal:  J Clin Immunol       Date:  2004-01       Impact factor: 8.317

2.  Immunological dysfunction, vaccination and Gulf War illness.

Authors:  Mark Peakman; Ania Skowera; Matthew Hotopf
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2006-04-29       Impact factor: 6.237

3.  Antigen-specific CD4+ T cells recognize epitopes of protective antigen following vaccination with an anthrax vaccine.

Authors:  Elsa M Laughlin; Joseph D Miller; Eddie James; Dimitri Fillos; Chris C Ibegbu; Robert S Mittler; Rama Akondy; William Kwok; Rafi Ahmed; Gerald Nepom
Journal:  Infect Immun       Date:  2007-02-05       Impact factor: 3.441

Review 4.  Adaptive Immune Responses Associated with the Central Nervous System Pathology of Gulf War Illness.

Authors:  Aurore Nkiliza; Utsav Joshi; James E Evans; Ghania Ait-Ghezala; Megan Parks; Fiona Crawford; Michael Mullan; Laila Abdullah
Journal:  Neurosci Insights       Date:  2021-05-25

5.  Evidence for abnormal cytokine expression in Gulf War Illness: A preliminary analysis of daily immune monitoring data.

Authors:  Luke Parkitny; Stephanie Middleton; Katharine Baker; Jarred Younger
Journal:  BMC Immunol       Date:  2015-09-30       Impact factor: 3.615

6.  Gastrointestinal problems in modern wars: clinical features and possible mechanisms.

Authors:  Wei-Feng Wang; Xiao-Xu Guo; Yun-Sheng Yang
Journal:  Mil Med Res       Date:  2015-06-24
  6 in total

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