4.3 Article

Multiple sclerosis patients show sexual dimorphism in cytokine responses to myelin antigens

期刊

JOURNAL OF NEUROIMMUNOLOGY
卷 193, 期 1-2, 页码 161-169

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jneuroim.2007.10.010

关键词

multiple sclerosis; inflammatory T-helper-1 (Th1); anti-inflammatory T-helper-2 (Th2); cytokines; sexual dimorphism; myelin

资金

  1. NATIONAL CENTER FOR RESEARCH RESOURCES [M01RR018390] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS041972] Funding Source: NIH RePORTER
  3. NCRR NIH HHS [M01 RR018390, M01 RR-018390] Funding Source: Medline
  4. NINDS NIH HHS [R01 NS041972, NIH R01 NS 41972, R01 NS041972-01, R01 NS041972-03, R01 NS041972-04A2, R01 NS041972-02] Funding Source: Medline
  5. PHS HHS [NMSS FA 1459-A-1] Funding Source: Medline
  6. CSR NIH HHS [NMSS RG 3263-A-3] Funding Source: Medline

向作者/读者索取更多资源

Multiple sclerosis affects more women than men. The reasons for this are unknown. Previously, we have shown significant differences in women versus men in inflammatory cytokine responses to the major protein component of myelin, proteolipid protein (PLP), which is thought to be a target in MS patients. Here, using the ELISPOT assay, we examined sex differences in single-cell secretion of Th1 and Th2 cytokines from freshly isolated PBMC between relapsing remitting (RR) MS patients and healthy individuals. Cells were stimulated with MS-associated antigens including proteolipid protein (PLP), myelin basic protein (MBP), myelin oligodendrocyte glycoprotein (MOG), and non-disease related antigens. Our data show a sex bias in the cytokine responses to multiple MS-relevant myelin antigens: Women with MS show IFN gamma-skewed responses and men with MS show IL-5-skewed responses. These data extend our previous findings [Pelfrey, C.M., Cotleur, A.C., Lee, J.C., Rudick, R.A. 2002. Sex differences in cytokine responses to myelin peptides in multiple sclerosis. J. Neuroimmunol. 130, 211-223.]: (1) by demonstrating gender skewing in cytokine responses to an expanded myelin antigen repertoire, which includes MBP, MOG and PLP; (2) by showing TNF alpha and IL-10 do not display comparable gender skewing compared to IFN gamma and IL5; (3) by defining the patient population as early, untreated RRMS patients to avoid confounding factors, such as different disease stages/disability and immunomodulatory therapy; and (4) by showing HLA type does not appear to underlie the gender differences. These findings may explain increased susceptibility to MS in women and could contribute to the differences in disease severity between men and women. (C) 2007 Elsevier B.V. All rights reserved.

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