Source: WASHINGTON STATE UNIVERSITY submitted to NRP
HAEMONCHUS CONTORTUS INTESTINAL MEMBRANE PROTEINS THAT INDUCE LOCAL CD4+ TH2 RESPONSES
Sponsoring Institution
National Institute of Food and Agriculture
Project Status
EXTENDED
Funding Source
Reporting Frequency
Annual
Accession No.
0200844
Grant No.
(N/A)
Cumulative Award Amt.
(N/A)
Proposal No.
(N/A)
Multistate No.
(N/A)
Project Start Date
Jul 1, 2004
Project End Date
Jun 30, 2006
Grant Year
(N/A)
Program Code
[(N/A)]- (N/A)
Recipient Organization
WASHINGTON STATE UNIVERSITY
240 FRENCH ADMINISTRATION BLDG
PULLMAN,WA 99164-0001
Performing Department
ANIMAL HEALTH RESEARCH CENTER
Non Technical Summary
Parasitic gastrointestinal nematodes cause significant losses in livestock production. This project will advance progress toward effective vaccination against gastrointestinal nematodes of production animals.
Animal Health Component
(N/A)
Research Effort Categories
Basic
100%
Applied
(N/A)
Developmental
(N/A)
Classification

Knowledge Area (KA)Subject of Investigation (SOI)Field of Science (FOS)Percent
31136201090100%
Knowledge Area
311 - Animal Diseases;

Subject Of Investigation
3620 - Meat, sheep;

Field Of Science
1090 - Immunology;
Goals / Objectives
The general objective of this research is to isolate and identify antigens from the parasitic nematode Haemonchus contortus that induce local (abomasal) CD4+ T lymphocyte responses during an infection. The specific goal is to isolate these antigens from intestinal membrane fractions of the worm, which has been shown to induce local CD4+ T lymphocyte responses. Antigens identified will be used in future immunization trials to protect small ruminants against infection.
Project Methods
Several fractionation schemes have been developed to isolate specific intestinal membrane proteins for testing. Methods to obtain CD4+ T lymphocytes that recognize intestinal membrane proteins have been established. Lymphocyte proliferation assays will be used to screen antigen fractions. Cytokine responses induced by those antigens will be measured using reverse transcriptase PCR. Our interest is to identify antigens that preferentially stimulate T helper 2 cytokines.