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Content archived on 2024-05-30

Deciphering the molecular basis of regulatory T cell suppression

Objective

Regulatory T cells (TREG) comprise a subset of CD4+ T cells that maintain immunological tolerance by suppressing immune activation in a dominant manner. TREG helps shaping the immune responses to autoantigens, alloantigens, tumors, pathogens and allergens, and are thus considered a therapeutical target in a large variety of diseases. One aspect of TREG biology that remains poorly understood is what molecular program(s) are induced in cells that are being actively suppressed by TREG. The specific aims described below are designed to provide a better understanding of the molecular changes that occur as a result of TREG-mediated suppression and determine if the biochemical pathways altered by TREG-mediated suppression can be exploited for therapeutical purposes.

1. Characterize the molecular changes that occur in CD4+ T cells and dendritic cells that are being suppressed by TREG using gene profiling and cell signaling experimental approaches.

2. Evaluate the importance and therapeutical potential of genes with an expression
profile altered by TREG-mediated suppression in animal models of human diseases.

Fields of science (EuroSciVoc)

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Keywords

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Topic(s)

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Call for proposal

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FP7-PEOPLE-IRG-2008
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Funding Scheme

Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.

MC-IRG - International Re-integration Grants (IRG)

Coordinator

KAROLINSKA INSTITUTET
EU contribution
€ 100 000,00
Address
NOBELS VAG 5
171 77 STOCKHOLM
Sweden

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Region
Östra Sverige Stockholm Stockholms län
Activity type
Higher or Secondary Education Establishments
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Total cost

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