Organ-specific heterogeneity in tumor-infiltrating immune cells and cancer antigen expression in primary and autologous metastatic lung adenocarcinoma

Abstract

Tumor immune microenvironment (TIME) and cancer antigen expression, key factors for the development of immunotherapies, are usually based on the data from primary tumors due to availability of tissue for analysis; data from metastatic sites and their concordance with primary tumor are lacking. Although of the same origin from primary tumor, organ-specific differences in the TIME in metastases may contribute to discordant responses to immune checkpoint inhibitor agents. In immunologically ‘cold’ tumors, cancer antigen-targeted chimeric antigen receptor (CAR) T-cell therapy can promote tumor-infiltrating lymphocytes; however, data on distribution and intensity of cancer antigen expression in primary tumor and matched metastases are unavailable.

Document Details

Document Type
Pub Defense Publication
Publication Date
Jun 01, 2023
Source ID
10.1136/jitc-2022-006609

Entities

People

  • Alexander J Byun
  • Carlos Thomas
  • David R Jones
  • David Restle
  • Jennie K. Choe
  • Joseph Dux
  • Kay See Tan
  • Kyohei Misawa
  • Navin K. Chintala
  • Prasad S Adusumilli
  • Raj G. Vaghjiani
  • Xiaoyu Li
  • Yan Li

Organizations

  • National Cancer Institute
  • United States Department of Defense

Tags

Fields of Study

  • Biology
  • Medicine

Readers

  • Immunology
  • Oncology (Cancer Research).
  • Regression Analysis.

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech