Anti-Search for the Glueball Candidate f_J(2220) in Two-Photon Interactions

Using 13.3 fb^{-1} of e^+e^- data recorded with the CLEO II and CLEO II.V detector configurations at CESR, we have searched for f_J(2220) decays to K^0_{S} K^0_{S} in untagged two-photon interactions. We report an upper limit on the product of the two-photon partial width and the branching fraction, Gamma_gamma gamma cdot B (f_J(2220) to K^0_{S} K^0_{S}) of less than 1.1 eV at the 95% C.L: systematic uncertainties are included. This dataset is four times larger than that used in the previous CLEO publication.Comment: 10 pages postscript, also available through http://w4.lns.cornell.edu/public/CLNS, Submitted to PRD (R

Further Experimental Studies of Two-Body Radiative \Upsilon Decays

Continuing our studies of radiative Upsilon(1S) decays, we report on a search for Upsilon to gamma eta and Upsilon to gamma f_{J}(2220) in 61.3 pb^{-1} of e^{+}e^{-} data taken with the CLEO II detector at the Cornell Electron Storage Ring. For the gamma eta search the three decays of the eta meson to pi^{+}pi^{-}pi^{0}, pi^{0}pi^{0}pi^{0}, and gamma gamma were investigated. We found no candidate events in the two (3\pi)^{0} modes and no significant excess over expected backgrounds in the gamma gamma mode to set a limit on the branching fraction of B(Upsilon to gamma eta) < 2.1 x 10^{-5} at 90% C.L. The three charged two-body final states h h-bar (h = pi^{+}, K^{+}, p) were investigated for f_{J}(2220) production, with one, one, and two events found, respectively. Limits at 90% C.L. of B(\Upsilon to gamma f_{J}) x B(f_{J} to h h-bar) ~ 1.5 x 10^{-5} have been set for each of these modes. We compare our results to measurements of other radiative Upsilon decays, to measurements of radiative J/psi decays, and to theoretical predictions.Comment: 19 pages postscript, also available through http://w4.lns.cornell.edu/public/CLNS, submitted to Physical Review

Regulation of VH gene repertoire and somatic mutation in germinal centre B cells by passively administered antibody

Immunization with T-dependent antigens induces a rapid differentiation of B cells to plasmacytes that produce the primary immunoglobulin M (IgM) and IgG antibodies with low affinities for the immunogen. It is proposed that the IgG antibody forms immune complexes with the residual antigen which provide an important stimulus for the formation of germinal centres (GC) and the activation of somatic mutation. This hypothesis was tested by passive administration of hapten-specific antibody into mice shortly after the immunization with nitrophenyl (NP) coupled to chicken gamma globulin (NP-CGG) in an environment of limited T-cell help. Athymic mice that received normal T helper cells at 72 hr after the administration of antigen produced low levels of anti-NP antibody and the splenic GC formation was delayed until day 12 after the antigen administration. The analysis of VDJ segments from NP-reactive GC B cells showed very few mutations in the VH genes. Passive injection of anti-NP IgG1 monoclonal antibody – but, not IgM – stimulated the GC formation up to normal levels and the somatic mutation activity in the GC B cells was fully restored. In addition, GC B cells in the recipients of IgG1 antibody demonstrated a change in the usage of germline-encoded VH genes which was not apparent among the primary antibody-forming cells. These results suggest the existence of a specific feedback mechanism whereby the IgG antibody regulates the GC formation, clonotypic repertoire and somatic mutation in GC B cells