The intricate relationship between autoimmunity disease and neutrophils death patterns: a love-hate story

Apoptosis. 2023 Oct;28(9-10):1259-1284. doi: 10.1007/s10495-023-01874-w. Epub 2023 Jul 24.

Abstract

Autoimmune diseases are pathological conditions that result from the misidentification of self-antigens in immune system, leading to host tissue damage and destruction. These diseases can affect different organs and systems, including the blood, joints, skin, and muscles. Despite the significant progress made in comprehending the underlying pathogenesis, the complete mechanism of autoimmune disease is still not entirely understood. In autoimmune diseases, the innate immunocytes are not functioning properly: they are either abnormally activated or physically disabled. As a vital member of innate immunocyte, neutrophils and their modes of death are influenced by the microenvironment of different autoimmune diseases due to their short lifespan and diverse death modes. Related to neutrophil death pathways, apoptosis is the most frequent cell death form of neutrophil non-lytic morphology, delayed or aberrant apoptosis may contribute to the development anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitis (AAV). In addition, NETosis, necroptosis and pyroptosis which are parts of lytic morphology exacerbate disease progression through various mechanisms in autoimmune diseases. This review aims to summarize recent advancements in understanding neutrophil death modes in various autoimmune diseases and provide insights into the development of novel therapeutic approaches for autoimmune diseases.

Keywords: Autoimmune diseases; Cell death; Inflammation; Neutrophil; Neutrophil extracellular traps; Pyroptosis.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis* / etiology
  • Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis* / pathology
  • Apoptosis
  • Autoimmune Diseases* / complications
  • Autoimmunity
  • Humans
  • Neutrophils