A gamma delta T-ceH hybridoma established from influenza virus-infecte
d mice responded in a reproducible way when cultured with influenza vi
rus-infected stimulators, Subclones of this line responded to cells in
fected with influenza viruses A/PR/8/34 (H1N1), S-31 (H3N2), and B/HK/
8/73 but not to cells infected with vaccinia virus or Sendai virus, Th
is spectrum of response to both type A and type B orthomyxoviruses has
never been recognized for the alpha beta T-cell receptor-positive sub
sets. There was no response to cells infected with a panel of recombin
ant vaccinia viruses expressing all individual influenza virus protein
s, and so it is unlikely that the stimulating antigen is of viral orig
in, The alternative is that the antigen is a cellular molecule induced
in influenza virus-infected cells, Infectious virus was required for
stimulation, and immunofluorescence studies showed increased expressio
n of heat shock protein 60 (Hsp60) in influenza virus but not Sendai v
irus- or vaccinia virus-infected cells, Both the hybridoma generated f
rom influenza virus-infected mice and an established hybridoma which u
ses the same gamma delta T-cell receptor combination responded to reco
mbinant Hsp60. Furthermore, the Hsp60-reactive hybridoma, which was ob
tained from an uninfected mouse, also responded to influenza virus-inf
ected cells, indicating that Hsp60 may indeed be the target antigen.