University of Surrey

Test tubes in the lab Research in the ATI Dance Research

Analysis of T-Helper Cell Epitopes on the Structural Glycoproteins of Venezuelan Encephalitis Virus.

Mathews, James H. (1993) Analysis of T-Helper Cell Epitopes on the Structural Glycoproteins of Venezuelan Encephalitis Virus. Doctoral thesis, University of Surrey (United Kingdom)..

[img]
Preview
Text
11012653.pdf
Available under License Creative Commons Attribution Non-commercial Share Alike.

Download (8MB) | Preview

Abstract

The T-helper (Th) cell immune response in mice to various alphaviruses and the structural envelope (E) glycoproteins E1 and E2 of Venezuelan equine encephalitis (VEE) TC-83 virus was investigated. Antigens analysed included the structural glycoproteins expressed in a recombinant vaccinia-VEE virus (TC-5A), sodium dodecyl sulfate-polyacrylamide gel electrophoresis separated E1 and E2, and synthetic peptides prepared from the extramembranal domain of the E2 and selected regions of the E1. Subunit peptides, prepared from the biologically important amino terminus (amino acids [AA] 1-25) of the E2 of VEE Trinidad donkey virus, were also analysed. Th cells from spleens of C3H, C57BL/6 or BALB/c mice immunized with virus, glycoprotein or free peptide and enriched by nylon wool chromatography were analysed for recognition of antigen in an in vitro lymphoblastogenesis test (LBT). The associated antibody response was also measured using an indirect enzyme-linked immunosorbent assay with the appropriate antigens. The predominant proliferating cell type in LBTs secreted IL-2 and was of the Th-cell phenotype Thy-1+, Lyt-1+, 2-, L3T4+. The LBT and antibody responses in C3H mice to VEE, western and eastern equine encephalitis viruses were primarily virus specific. The Th-cell response to the recombinant TC-5A virus was similar to that seen with VEE virus. VEE virus Th cells recognized both the E2 and E1 glycoproteins in LBT and the glycoproteins were able to prime mice for an anamnestic antibody response to conformationally dependent B-cell epitopes present on the challenge VEE virus. E2 and E1 synthetic peptides defined various immunodominant virus-reactive Th-cell epitopes, and genetic restriction of the immune response was seen. The subunit peptides defined multiple Th- and B-cell elements and a dominant Th-cell epitope was found in peptide S3 (AA 9-19). The results from this study indicate that both the E1 and E2 glycoproteins contain Th-cell epitopes of biological importance and that a single residue interchange can alter the expression of both Th- and B-cell epitopes.

Item Type: Thesis (Doctoral)
Divisions : Theses
Authors : Mathews, James H.
Date : 1993
Additional Information : Thesis (Ph.D.)--University of Surrey (United Kingdom), 1993.
Depositing User : EPrints Services
Date Deposited : 30 Apr 2019 08:08
Last Modified : 20 Aug 2019 15:32
URI: http://epubs.surrey.ac.uk/id/eprint/851405

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year


Information about this web site

© The University of Surrey, Guildford, Surrey, GU2 7XH, United Kingdom.
+44 (0)1483 300800