The Fine Specificity and Cytokine Profile of T-Helper Cells ... : Journal of the American Society of Nephrology (original) (raw)
Immunology and Pathology
The Fine Specificity and Cytokine Profile of T-Helper Cells Responsive to the α3 Chain of Type IV Collagen in Goodpasture’s Disease
Cairns, Lindsay S.*; Phelps, Richard G.†; Bowie, Laura*; Hall, Andrew M.*; Saweirs, Walaa W.M.†; Rees, Andrew J.*; Barker, Robert N.*
*Department of Medicine and Therapeutics, University of Aberdeen, Aberdeen, United Kingdom; and *Department of Clinical and Surgical Sciences (Internal Medicine), University of Edinburgh, Edinburgh, United Kingdom
Correspondence to Dr. Robert N. Barker, Department of Medicine and Therapeutics, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, United Kingdom. Phone: +44-1224-273168; Fax: +44-1224-273066;
Accepted July 24, 2003
Received May 01, 2002
Abstract
Goodpasture’s disease is a severe nephritis characterized by autoantibodies to the α3 chain of type IV collagen, α3(IV)NC1, in the glomerular basement membrane. The disease is very strongly associated with HLA-DR15, the affinities of α3(IV)NC1 peptides for DR15 are known, and elution experiments have identified major naturally processed sequences. Here, the fine specificity and cytokine profile of α3(IV)NC1-reactive T cells from patients with Goodpasture’s disease is defined. Peripheral blood mononuclear cells from patients at diagnosis proliferated in response to significantly more peptides (χ2 = 8.6, P = 0.004) from a panel spanning the sequence of α3(IV)NC1 than did those from control DR15-positive donors and were highly focused (P = 0.0002, binomial distribution) on two peptides, α371–90 and α3131–150. Some peptides induced interferon-γ, but none induced IL-4. Resolution of disease was accompanied by a striking deviation of the responses from proliferation to secretion of the T-regulatory cytokine IL-10, and addition of neutralizing antibody confirmed that such IL-10 production was suppressive. The affinity of the peptides for DR15 molecules was positively correlated (χ2 = 14.6, P = 0.00067) with the ability to elicit proliferation. However, unlike foreign antigens, this hierarchy is not due to responses against the major naturally processed peptides, which rarely stimulated proliferation and which have only intermediate affinity for DR15 molecules. It is inferred that the helper response to α3(IV)NC1 in Goodpasture’s disease is dominated by epitopes that are normally inefficiently presented because of processing constraints. E-mail: [email protected]
Copyright © 2003 The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved.