Lung injury combined with loss of regulatory T cells leads to de novo lung-restricted autoimmunity

Stephen Chiu, Ramiro Fernandez, Vijay Subramanian, Haiying Sun, Malcolm M. DeCamp, Daniel Kreisel, Harris Perlman, G. R.Scott Budinger, Thalachallour Mohanakumar, Ankit Bharat*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

20 Scopus citations


More than one third of patients with chronic lung disease undergoing lung transplantation have pre-existing Abs against lungrestricted self-Ags, collagen type V (ColV), and k-a1 tubulin (KAT). These Abs can also develop de novo after lung transplantation and mediate allograft rejection. However, the mechanisms leading to lung-restricted autoimmunity remain unknown. Because these self-Ags are normally sequestered, tissue injury is required to expose them to the immune system.We previously showed that respiratory viruses can induce apoptosis in CD4+CD25+Foxp3+ regulatory T cells (Tregs), the key mediators of self-tolerance. Therefore, we hypothesized that lung-tissue injury can lead to lung-restricted immunity if it occurs in a setting when Tregs are impaired.We found that human lung recipients who suffer respiratory viral infections experienced a decrease in peripheral Tregs. Pre-existing lung allograft injury from donor-directed Abs or gastroesophageal reflux led to new ColV and KATAbs post respiratory viral infection. Similarly, murine parainfluenza (Sendai) respiratory viral infection caused a decrease in Tregs. Intratracheal instillation of anti-MHC class I Abs, but not isotype control, followed by murine Sendai virus infection led to development of Abs against ColV and KAT, but not collagen type II (ColII), a cartilaginous protein. This was associated with expansion of IFN-g-producing CD4+ T cells specific to ColVand KAT, but not ColII. Intratracheal anti-MHC class I Abs or hydrochloric acid in Foxp3-DTR mice induced ColV and KAT, but not ColII, immunity, only if Tregs were depleted using diphtheria toxin.We conclude that tissue injury combined with loss of Tregs can lead to lung-tissue-restricted immunity.

Original languageEnglish (US)
Pages (from-to)51-57
Number of pages7
JournalJournal of Immunology
Issue number1
StatePublished - Jul 1 2016

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology


Dive into the research topics of 'Lung injury combined with loss of regulatory T cells leads to de novo lung-restricted autoimmunity'. Together they form a unique fingerprint.

Cite this