Genetic elimination of CD43 has been associated with increased T cell adhes
iveness and T cell hyperresponsiveness to mitogens and alloantigens, Theref
ore, we investigated whether T cell development was perturbed in CD43-defic
ient mice by breeding CD43(null) mice with male Ag (Hy)-specific TCR-transg
enic mice. Neither positive nor negative thymic selection of male Ag-specif
ic T cells were affected by CD43 status. Furthermore, we did not observe a
substantial or consistent hyperresponsive pattern in HY-CD43(null) lymph no
de cells compared with littermate HY-CD43(+/-) lymph node cells upon analys
is of in vitro T cell stimulation with male Ag or mitogen, These observatio
ns challenged original conclusions associating absence of CD43 with T cell
hyperresponsiveness and led us to re-examine this association, Reported phe
notypes of CD43(null) mice have been based on mice with a mixed 129xC57BL/6
genetic background. To exclude a possible influence of genetic background
differences among individual mice we analyzed CD43(null) littermates that h
ad been back-bred onto the C57BL/6 background for seven to eight generation
s. We found that CD43(+) and CD43(null) littermates with the C57BL/6 backgr
ound exhibited no differences in response to mitogen or alloantigen, thereb
y establishing that T cell hyperresponsiveness is not a general correlate o
f CD43 absence.