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DBSP Faculty

Dr. Steven Holladay

Steven D. Holladay, MS, PhD

Professor
Toxicology, Pharmacology
Department of Biomedical Sciences & Pathobiology
 
e-mail: holladay@vt.edu

Education

1989 Ph.D, Toxicology/Pharmacology
North Carolina State University
1984 M.S., Physiology
North Carolina State University

Research Interests

Developmental exposure of SNF1 mice to TCDD induces and exacerbates postnatal autoimmune lupus-like nephritis. Mechanisms that may singly or collectively underlie this environmental chemical effect on immune development are a focus of our research. These include:

  • impaired deletion of autoreactive T cell clones in the thymus;
  • diminished regulatory T cells that control inappropriate responses to self antigen;
  • the forcing of T cell differentiation into extra-thymic compartments where negative selection is inefficient;
  • a shift in the postnatal T cell repertoire toward a T helper profile and antibody production;
  • and inappropriate B cell activity including autoantibody production.

Present experiments are examining numbers of T cells expressing autoreactive CD4+ V—_17a+ and CD3+ V—_3+ TcR, and numbers of CD4+25+ regulatory T cells, in extrathymic and thymic compartments, over postnatal time in SNF1 mice (autoimmune-predisposed but TCDD insensitive) and correlated to disease progression. C57Bl/6 mice (non-autoimmune but TCDD sensitive) are being used in parallel for risk assessment considerations in individuals who may be both sensitive to TCDD and genetically predisposed to autoimmune disease.
 
In both SNF1 and C57Bl/6 mice: Con A stimulated splenic lymphocytes are being evaluated over postnatal time to identify chemical-imprinted shifts in cytokine production that may precipitate or exacerbate the postnatal autoantibody response. Antibody level to ssDNA, dsDNA and cardiolipin is being determined for comparison to cytokine profile and T helper cell activity. A focused autoimmunity gene array consisting of appropriate response genes will be used to determine the postnatal integrity of fundamental signaling pathways, proteins and downstream targets of signal transduction pathways that mediate the immune response. A reverse transcription PCR-based differential display will be used to examine thymic MHC class I and II gene expression in SNF1 and C57Bl/6 mice, with or without TCDD exposure during gestation, as a mechanism that may impair T cell education and increase peripheral autoreactive cells.
 
These collective experiments are designed to detect alterations in fetal immune development caused by TCDD, that underlie the worsened postnatal (post-pubertal) autoimmune disease caused by this chemical.

Professional Experience

1992-present Professor
VMRCVM, Virginia Tech
1991-1992 Assistant Professor
North Carolina State University
1990-1991 NIEHS Post doctoral