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Bone Marrow Core Biopsy Adequacy and Variability in the United Stated and Canada: A Multicenter Retrospective Study [Meeting Abstract]

Merzianu, Mihai; Cheney, Richard; Groman, Adrienne; Deeb, George; Wilding, Gregory; Cotta, Claudiu; Amre, Ramila; Balasubramanian, Manjula; Brandao, Guilherme; Brynes, Russell K.; Cherian, Sindhu; Courville, Elizabeth; Czuchlewski, David; Fan, Guang; Grier, David; Hoehn, Daniela; Hutchison, Robert E.; Inamdar, Kedar V.; Juskevicius, Ridas; Kaur, Prabhjot; Lazarchick, John; Lewis, Michael R.; Miles, Rodney R.; Myers, Jerome B.; Nasr, Michel; Naushad, Hina; Olteanu, Horatiu; Orazi, Attilio; Reddy, Vishnu V. B.; Robu, Valentin G.; Salaru, Gratian; Teruya-Feldstein, Julie; Vajpayee, Neerja; Vos, Jeffrey; Zhang, Ling; Zhang, Shanxing; Sedelmeyer, Ashley V.; Arguello, Vivian; Aye, Le; Barouk, Sharon; Brega, Elisa F.; Carpenter, Richie; Coad, James E.; DiPonio, Alana; Garcia, Fernandez; Grantham, John; Ivelja, Sinisa; McKenna, Robert; Sultan, Kieran; Thomsen, Matthew B.; Xu, Jie; Peterson, Loann; Neppalli, Vishala T.
ISSN: 0006-4971
CID: 4727982

Targeted depletion of lymphotoxin-alpha-expressing TH1 and TH17 cells inhibits autoimmune disease

Chiang, Eugene Y; Kolumam, Ganesh A; Yu, Xin; Francesco, Michelle; Ivelja, Sinisa; Peng, Ivan; Gribling, Peter; Shu, Jean; Lee, Wyne P; Refino, Canio J; Balazs, Mercedesz; Paler-Martinez, Andres; Nguyen, Allen; Young, Judy; Barck, Kai H; Carano, Richard A D; Ferrando, Ron; Diehl, Lauri; Chatterjea, Devavani; Grogan, Jane L
Uncontrolled T helper type 1 (T(H)1) and T(H)17 cells are associated with autoimmune responses. We identify surface lymphotoxin-alpha (LT-alpha) as common to T(H)0, T(H)1 and T(H)17 cells and employ a unique strategy to target these subsets using a depleting monoclonal antibody (mAb) directed to surface LT-alpha. Depleting LT-alpha-specific mAb inhibited T cell-mediated models of delayed-type hypersensitivity and experimental autoimmune encephalomyelitis. In collagen-induced arthritis (CIA), preventive and therapeutic administration of LT-alpha-specific mAb inhibited disease, and immunoablated T cells expressing interleukin-17 (IL-17), interferon-gamma and tumor necrosis factor-alpha (TNF-alpha), whereas decoy lymphotoxin-beta receptor (LT-betaR) fusion protein had no effect. A mutation in the Fc tail, rendering the antibody incapable of Fcgamma receptor binding and antibody-dependent cellular cytotoxicity activity, abolished all in vivo effects. Efficacy in CIA was preceded by a loss of rheumatoid-associated cytokines IL-6, IL-1beta and TNF-alpha within joints. These data indicate that depleting LT-alpha-expressing lymphocytes with LT-alpha-specific mAb may be beneficial in the treatment of autoimmune disease.
PMID: 19561618
ISSN: 1546-170x
CID: 4727922

The surface protein TIGIT suppresses T cell activation by promoting the generation of mature immunoregulatory dendritic cells

Yu, Xin; Harden, Kristin; Gonzalez, Lino C; Francesco, Michelle; Chiang, Eugene; Irving, Bryan; Tom, Irene; Ivelja, Sinisa; Refino, Canio J; Clark, Hilary; Eaton, Dan; Grogan, Jane L
Here we have identified a surface protein, TIGIT, containing an immunoglobulin variable domain, a transmembrane domain and an immunoreceptor tyrosine-based inhibitory motif that was expressed on regulatory, memory and activated T cells. Poliovirus receptor, which is expressed on dendritic cells, bound TIGIT with high affinity. A TIGIT-Fc fusion protein inhibited T cell activation in vitro, and this was dependent on the presence of dendritic cells. The binding of poliovirus receptor to TIGIT on human dendritic cells enhanced the production of interleukin 10 and diminished the production of interleukin 12p40. Knockdown of TIGIT with small interfering RNA in human memory T cells did not affect T cell responses. TIGIT-Fc inhibited delayed-type hypersensitivity reactions in wild-type but not interleukin 10-deficient mice. Our data suggest that TIGIT exerts immunosuppressive effects by binding to poliovirus receptor and modulating cytokine production by dendritic cells.
PMID: 19011627
ISSN: 1529-2916
CID: 4727912