Antibodies specific for disease-associated antigens (DAA) expressed in non-malignant diseases reveal potential new tumor-associated antigens (TAA) for immunotherapy or immunoprevention

Semin Immunol. 2020 Feb:47:101394. doi: 10.1016/j.smim.2020.101394. Epub 2020 Apr 6.

Abstract

Immune responses to a large number of mutated and non-mutated tumor antigens have been studied in an attempt to unravel the highly complex immune response to cancer. Better understanding of both the effectors and the targets of successful immunosurveillance can inform various immunotherapeutic approaches, which can strengthen or replace natural immunosurveillance that a tumor has managed to escape. In this review we highlight targets of antibodies generated in the context of diseases other than cancer, such as asthma, allergies, autoimmune disorders, inflammation and infections, where the antibody presence correlates either with an increased or a reduced lifetime risk of cancer. We focus on their target antigens, self-molecules abnormally expressed on diseased cells or cross-reactive with exogenous antigens and found on cancer cells as tumor associated antigens (TAA). We refer to them as disease-associated antigens (DAA). We review 4 distinct categories of antibodies according to their target DAA, their origin and their reported impact on cancer risk: natural antibodies, autoantibodies, long-term memory antibodies and allergy-associated antibodies. Increased understanding and focus on their specific targets could enable a more rational choice of antigens for both therapeutic and preventative cancer vaccines and other more effective and less toxic cancer immunotherapies.

Keywords: Autoantibodies; Immunotherapy; Inflammation; Molecular mimicry; Natural antibodies.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Antibodies / genetics*
  • Antibodies / immunology*
  • Antigens, Neoplasm / immunology*
  • Autoantibodies / immunology
  • Disease Management
  • Disease Susceptibility
  • Humans
  • Hypersensitivity / immunology
  • Immunoglobulin E / immunology
  • Immunotherapy* / adverse effects
  • Immunotherapy* / methods
  • Microbiota
  • Molecular Mimicry
  • Neoplasms / immunology*
  • Neoplasms / pathology
  • Neoplasms / prevention & control
  • Neoplasms / therapy*
  • Precancerous Conditions
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism

Substances

  • Antibodies
  • Antigens, Neoplasm
  • Autoantibodies
  • Immunoglobulin E