Control of Disease Recurrence by Tumor-Infiltrating T Cells in Ovarian Cancer

Abstract

Ovarian cancer patients with large numbers of T cells in their tumor live longer after chemotherapy compared to patients with fewer T cells in their tumor. Our goal is to use modern genomic techniques to identify the antigens recognized by these T cells, with an emphasis on new antigens that arise during chemotherapy. To this end, we are collecting matched primary and recurrent tumor tissue from ovarian cancer patients (Tasks 1-2); this is progressing well. The antigen receptors expressed by tumor-infiltrating T cells (Task 2) and B cells (Task 3) have been identified in several patients by DNA sequencing methods. Primary and recurrent tumor tissue from one patient has been analyzed by whole exome sequencing, and a large number of candidate mutations have been identified (Task 4). Finally, new methods have been developed to rapidly test the recognition of tumor mutations by T cells from patients (Task 5). Overall, this project is progressing on schedule and is yielding publishable results and leveraged funding.

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Document Details

Document Type
Technical Report
Publication Date
Mar 01, 2011
Accession Number
ADA549144

Entities

People

  • Brad H Nelson

Organizations

  • BC Cancer Agency

Tags

DTIC Thesaurus Topics

  • Autoimmune Diseases
  • Blood
  • Breast Cancer
  • Carcinoma
  • Cardiovascular System
  • Cells
  • Chemistry
  • Gene Expression
  • Genetic Code
  • Genetic Structures
  • Genetics
  • Lymphatic Diseases
  • Lymphatic System
  • Lymphocytes
  • Oncology
  • Tissues
  • Transplants

Fields of Study

  • Biology
  • Medicine

Readers

  • Immunology
  • Oncology and Biomarker-Based Cancer Detection.
  • Women's Health and Cancer Risk Research: African American Women and Pregnancy Outcomes.