4.7 Article

Reactive murine lymph nodes uniquely permit parenchymal access for T cells that enter via the afferent lymphatics

Journal

JOURNAL OF PATHOLOGY
Volume 226, Issue 5, Pages 806-813

Publisher

WILEY-BLACKWELL
DOI: 10.1002/path.3975

Keywords

lymph nodes; T cells; cell migration; lymphatic sinuses; high endothelial venules; viral infection; HSV

Funding

  1. Swedish Research Council
  2. Swedish Society of Medicine
  3. Fernstrom Foundation
  4. Australian National Health and Medical Research Council (NHMRC)
  5. Australian Research Council (ARC)

Ask authors/readers for more resources

Whereas naive T cells access the lymph nodes predominantly via the high endothelial venules, their effector counterparts can also enter via the afferent lymphatics. It is unclear if such cells are confined to the lymphatic spaces during their transit through the lymph node or whether they can access the lymphocyte- and dendritic cell-rich parenchyma with its potentially stimulatory environment. We used a flank HSV inoculation model that featured neuronal-mediated movement of virus to distinct areas of skin to study the lymphatic-mediated transit of activated T cells between different skin-draining lymph nodes. These experiments showed that activated T cells released from the brachial lymph node, draining the primary site of inoculation, entered the downstream axillary lymph node. These activated T cells accessed the subcapsular areas of the axillary lymph node via lymphatic vessels exiting the upstream brachial node regardless of whether the former drained skin that was associated with active infection. However, T cells remained within the sinusoidal network of the axillary lymph node unless it was directly associated with peripheral infection. Thus, activated T cells that enter a given lymph node using the afferent lymphatics do not have automatic access to the parenchyma unless it is a reactive node involved with peripheral inflammation or infection. Copyright (c) 2012 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available