The purpose of the present studies was to determine whether acute vaginal i
nfection with Herpes virus 2 altered the vaginal population of gamma delta
T cells, and whether gamma delta T cells influenced the vaginal clearance o
f HSV-2. BALB/c mice were infected intravaginally with the progressively le
thal wild type 333 strain, or the non-lethal thymidine kinase deficient (De
lta TK--HSV-2) mutant strain of HSV-2 virus. Changes in vaginal T cell comp
osition were examined by FACS analysis 4 days after infection. Clearance of
vaginal Delta TK--HSV-2 infection was compared between mice with normal ga
mma delta T cell populations (BALB/c) and transgenic mice in which all the
gamma delta T cells express a receptor that is specific for the b allotype
of MHC class Ib T10 antigen (G8/BALB/c). In HSV-2 infected BALB/c mice, but
not G8/BALB/c, a subset of gamma delta T cells that express a V gamma 2 TC
R accumulated in the Vaginal mucosa by the fourth day after infection. Unex
pectedly, we found that gamma delta TCR transgenic mice exhibited a more ra
pid clearance of the virus than control mice (P < 0.05). These findings arg
ue against the hypothesis that the normal populations of vaginal intraepith
elial gamma delta T cells play a direct role in the elimination of virally
infected epithelial cells. (C) 1999 Elsevier Science B.V. All rights reserv
ed.