Toll-like receptors, innate immunity and lung transplantation

Front Biosci (Elite Ed). 2009 Jun 1;1:600-4. doi: 10.2741/e58.

Abstract

Lung transplant allografts have the highest rate of rejection and shortest graft survival time among the commonly transplanted solid organs despite high levels of immunosuppression. This observation strongly indicates that mechanisms unique to the lung allograft contribute to rejection post lung transplant. Unlike most other solid organ recipients, the lung allograft is exposed to both the external environment and a significant amount of donor-derived lymphatic and structural tissue. For these reasons, the recipient's innate immune system may be critically involved in the initiation and maintenance of rejection after lung transplant. The strongest evidence for innate immune activation participating in lung allograft rejection is based upon genetic studies which demonstrate that variation in toll-like receptors and the related molecule CD14 modulate posttransplant lung allograft rejection. However, secreted pathogen recognition receptors, including defensins and collectins, and complement are parts of the innate pulmonary host defense and may be important in lung transplant rejection. This report will review the current understanding of innate immunity in lung allograft rejection in both murine and human studies.

Publication types

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

MeSH terms

  • Animals
  • Collectins / immunology
  • Collectins / metabolism
  • Complement System Proteins / immunology
  • Complement System Proteins / metabolism
  • Defensins / immunology
  • Defensins / metabolism
  • Graft Rejection / immunology*
  • Humans
  • Immunity, Innate / immunology*
  • Lipopolysaccharide Receptors / immunology
  • Lipopolysaccharide Receptors / metabolism*
  • Lung Transplantation / immunology*
  • Mice
  • Toll-Like Receptors / immunology
  • Toll-Like Receptors / metabolism*

Substances

  • Collectins
  • Defensins
  • Lipopolysaccharide Receptors
  • Toll-Like Receptors
  • Complement System Proteins