Author
Listed:
- Clare L. V. Westhorpe
(Monash Medical Centre)
- M. Ursula Norman
(Monash Medical Centre)
- Pam Hall
(Monash Medical Centre)
- Sarah L. Snelgrove
(Monash Medical Centre)
- Michaela Finsterbusch
(Monash Medical Centre
Medical University of Vienna)
- Anqi Li
(Monash Medical Centre)
- Camden Lo
(Monash University)
- Zhe Hao Tan
(Monash Medical Centre)
- Songhui Li
(CSIRO Manufacturing
Monash University)
- Susan K. Nilsson
(CSIRO Manufacturing
Monash University)
- A. Richard Kitching
(Monash Medical Centre
Monash Medical Centre)
- Michael J. Hickey
(Monash Medical Centre)
Abstract
Although effector CD4+ T cells readily respond to antigen outside the vasculature, how they respond to intravascular antigens is unknown. Here we show the process of intravascular antigen recognition using intravital multiphoton microscopy of glomeruli. CD4+ T cells undergo intravascular migration within uninflamed glomeruli. Similarly, while MHCII is not expressed by intrinsic glomerular cells, intravascular MHCII-expressing immune cells patrol glomerular capillaries, interacting with CD4+ T cells. Following intravascular deposition of antigen in glomeruli, effector CD4+ T-cell responses, including NFAT1 nuclear translocation and decreased migration, are consistent with antigen recognition. Of the MHCII+ immune cells adherent in glomerular capillaries, only monocytes are retained for prolonged durations. These cells can also induce T-cell proliferation in vitro. Moreover, monocyte depletion reduces CD4+ T-cell-dependent glomerular inflammation. These findings indicate that MHCII+ monocytes patrolling the glomerular microvasculature can present intravascular antigen to CD4+ T cells within glomerular capillaries, leading to antigen-dependent inflammation.
Suggested Citation
Clare L. V. Westhorpe & M. Ursula Norman & Pam Hall & Sarah L. Snelgrove & Michaela Finsterbusch & Anqi Li & Camden Lo & Zhe Hao Tan & Songhui Li & Susan K. Nilsson & A. Richard Kitching & Michael J. , 2018.
"Effector CD4+ T cells recognize intravascular antigen presented by patrolling monocytes,"
Nature Communications, Nature, vol. 9(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-03181-4
DOI: 10.1038/s41467-018-03181-4
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