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Human gamma/delta T-cell proliferation and IFN-gamma production induced by hexamethylene diisocyanate.

Authors
Wisnewsk-AV; Herrick-CA; Liu-Q; Chen-L; Bottomly-K; Redlich-CA
Source
J Allergy Clin Immunol 2003 Sep; 112(3):538-546
NIOSHTIC No.
20029273
Abstract
The human immune response to isocyanate, a leading cause of occupational asthma, remains incompletely characterized, including the cell types involved and the form of the chemical that acts as an antigen. The purpose of this investigation was to characterize human T cells that respond to hexamethylene diisocyanate (HDI), an aliphatic isocyanate routinely used in the automobile body industry. Human T-cell lines were generated and characterized from peripheral blood of HDI-exposed and HDI-unexposed subjects, using two different HDI antigens, HDI-conjugated albumin and HDI-exposed human airway epithelial cells (NCI-H292). Flow cytometry was used to characterize the phenotype of HDI-responsive T cells. ELISA and intracellular staining techniques were used to evaluate HDI-induced cytokine production. DNA sequence analysis of T-cell receptors was used to further define clonal populations of HDI-responsive T cells. HDI antigen preparations but not "mock exposed" control antigens lead to increased proliferation of specific cell types, CD3+CD4-CD8(dim) and/or CD3+CD4-CD8- cells, from HDI-exposed but not from HDI-unexposed subjects. These HDI-responsive T cells expressed unique oligoclonal gamma/delta rather than alpha/beta T-cell receptors, with characteristics suggestive of antigen-mediated selection and specificity. The HDI-stimulated gamma/delta T cells were associated with T(H)1-like cytokines and produce IFN-gamma but not IL-5 or IL-13. These data are the first to demonstrate that HDI can selectively stimulate gamma/delta T cells with the potential to modulate the human immune response to exposure.
Keywords
Immune-reaction; Isocyanates; Occupational-diseases; Bronchial-asthma; Automotive-industry; Automobile-repair-shops; Allergens; Cell-division; Genes; Pulmonary-system-disorders
Contact
Adam V. Wisnewski, PhD, Department of Internal Medicine, Immunobiology and Dermatology, Yale School of Medicine, 333 Cedar Street, New Haven, CT 06520, USA
CODEN
JACIBY
Publication Date
20030901
Document Type
Journal Article
Funding Amount
2634676
Funding Type
Grant
Fiscal Year
2003
NTIS Accession No.
NTIS Price
Identifying No.
Grant-Number-R01-OH-003457
Issue of Publication
3
ISSN
0091-6749
Priority Area
Disease and Injury: Asthma and Chronic Obstructive Pulmonary Disease
Source Name
Journal of Allergy and Clinical Immunology
State
CT
Performing Organization
Yale University, New Haven, Connecticut
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