N.J. Custis
University of Virginia
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Publication
Featured researches published by N.J. Custis.
Journal of Immunology | 2004
Amanda J. Reefer; Raquel M. Carneiro; N.J. Custis; Thomas A.E. Platts-Mills; Sun-Sang J. Sung; Juergen Hammer; Judith A. Woodfolk
Although high dose exposure to inhaled cat allergen (Fel d 1) can cause a form of tolerance (modified Th2 response), the T cell mechanism for this phenomenon has not been studied. T cell responses to Fel d 1 were characterized in both allergic (IgEpos) and modified Th2 (IgEnegIgGpos) responders as well as serum Ab-negative controls (IgEnegIgGneg). Fel d 1 stimulated high levels of IL-10 in PBMC cultures from all individuals, with evidence of Th2 and Th1 cytokine skewing in allergic and control subjects, respectively. Using overlapping peptides, epitopes at the N terminus of Fel d 1 chain 2 were shown to stimulate strong T cell proliferation and to preferentially induce IL-10 (peptide 2:1 (P2:1)) or IFN-γ (P2:2) regardless of the allergic status of the donor. Injection of cat extract during conventional immunotherapy stimulated expansion of IL-10- and IFN-γ-producing chain 2 epitope-specific T cells along with increased Fel d 1-specific serum IgG and IgG4 Ab. Six of 12 modified responders expressed the major HLA-DRB1 allele, *0701, and both P2:1 and P2:2 were predicted ligands for this allele. Cultures from DR7-positive modified responders produced the highest levels of IL-10 to P2:1 in addition to other major and minor epitopes within chains 1 and 2. In the presence of anti-IL-10 mAb, both T cell proliferation and IFN-γ production were enhanced in a Fel d 1- and epitope-specific manner. We conclude that IL-10-producing T cells specific for chain 2 epitopes are relevant to tolerance induction, and that DR7-restricted recognition of these epitopes favors a modified Th2 response.
Clinical & Experimental Allergy | 2003
N.J. Custis; Judith A. Woodfolk; John W. Vaughan; T.A.E. Platts-Mills
Background Increasing evidence suggests that children raised with an animal(s) in the house have a decreased risk of becoming sensitized. However, it is not clear whether this phenomenon is related to airborne exposure.
The Journal of Allergy and Clinical Immunology | 2005
Elizabeth A. Erwin; Kristin Wickens; N.J. Custis; Robert Siebers; Judith A. Woodfolk; D. Barry; Julian Crane; Thomas A.E. Platts-Mills
The Journal of Allergy and Clinical Immunology | 2005
Elizabeth A. Erwin; N.J. Custis; S.M. Satinover; Matthew S. Perzanowski; Judith A. Woodfolk; Julian Crane; Kristin Wickens; Thomas A.E. Platts-Mills
The Journal of Allergy and Clinical Immunology | 2005
James A. Platts-Mills; N.J. Custis; Judith A. Woodfolk; Thomas A.E. Platts-Mills
Indoor Air | 2005
Elizabeth A. Erwin; N.J. Custis; E. Ronmark; Kristin Wickens; R. Sporik; Judith A. Woodfolk; T.A.E. Platts-Mills
Journal of Investigative Dermatology | 2004
Raquel M. Carneiro; Amanda J. Reefer; Barbara B. Wilson; Juergen Hammer; Thomas A.E. Platts-Mills; N.J. Custis; Judith A. Woodfolk
The Journal of Allergy and Clinical Immunology | 2004
James A. Platts-Mills; N.J. Custis; A. Kenney; Martin D. Chapman; A. Tsay; T.A.E. Platts-Mills
The Journal of Allergy and Clinical Immunology | 2003
Elizabeth A. Erwin; D.M. Riposo; Kristin Wickens; D. Barry; N.J. Custis; Julian Crane; T.A.E. Platts-Mills
The Journal of Allergy and Clinical Immunology | 2004
N.J. Custis; Judith A. Woodfolk; T.A.E. Platts-Mills