Immunity to mycobacterial infection (PP-061)

Autor: N. Aydin, I. Dambuza, N. Green, C. Guillen-Vargas, G. Hewinson, K. Takao, C. Sabio y García, S. H. E. Kaufmann, A. Zavvaran Hossieni, R. J. Wilkinson, N. Esphandyari, J. Cho, C. Nunes-Alves, S. Haga, M. Santiago-Maldonado, D. N. McMurray, M. R. Klein, K. Ishihara, E. N. Tsiganov, B. Paternesi, R. Tadokera, A. Shams, Renana Peres, Y. Kim, L. C. Rosa, T. L. Elvang, G. Maartens, S. Yoshida, K. Matthews, P. Court, T Mousavi, K. Forti, M. Jacobs, M. Sasiain, M. S. Shaila, M. H. Vordermeier, H. Hisaeda, K. Fatema, Y. Jung, J. Paluch-Oleś, J. Bourkadi, T. C. Martins, A. Pawlowski, I. Y. Konakova, A. R. Villasmil, P. Govender, A. Magryś, G. Gelsomino, P. Schierloh, J. Milanowski, D. McMurray, S. Yamamoto, D. M. Begum, R. Billeskov, C. Yenisey, Y. O. Yoshida, R. Strong, V. Ogando, M. Cagiola, D. J. Miles, C. McFarland, I. Ulea, K. Takatsu, B. Mishra, S. K. Jeong, P. van Weeren, S. Kumar, T. H. Flo, S. F. G. Zorzella-Pezavento, T. J. Scriba, A. Dorhoi, K. E. van Meijgaarden, A. Kariyone, J. Russell, G. Walzl, L. G. Popa, J. Mitchell, Prabhat K. Sharma, M. Fafutis-Morris, J. Vani, K. Tsuchiya, S. Gilbert, F. Shahsavar, G. Kallenius, N. Capan, S. Buus, S. Sakai, S. Hashimoto, P. Mazzone, A. Sartori, T. Tamura, Tom H. M. Ottenhoff, M. Akil, F. Escudero-Gutierrez, J. Dietrich, S. T. Tang, R. Seldon, S. Nishimatsu, C. Leepiyasakulchai, H. Dalan, A. G. Rosas-Taraco, J. C. Hope, Y. Suzaki, Y. Ami, B. Peixoto, J. Basu, J. H. Bae, S. Matsumoto, J. Bayry, Y. Ozeki, B. Ryffel, S. Lacroix-Desmazes, A. A. Pathan, T. Zaborowski, M. Okada, M. Haug, A. Alvarado, L. Ignatowicz, H. R. Stavri, F. Seghrouchni, M. S. Alam, M. Sekkat, J. Maeyama, B. M. Mayosi, J. E. Hughes, Y. Goto, S. Park, P. Andersen, Samuel M. Behar, Dipendra K. Mitra, K. C. Fae, S. V. Kaveri, S. A. Nedospasov, V. Ritacco, R. Keeton, A. V. S. Hill, N. Asadi, I. Kawamura, M. G. Aydin, E. Beser, M. T. Fernandez-Mestre, F. Syed, I. A. Vasilyeva, B. M. N. Kagina, G. Murgoci, F. Kazi, G. A. Meintjes, M. S. Viegas, M. Umemura, A. Erturk, C. Espitia-Pinzón, E. Ayaslioglu, Z. Layrisse, M. C. Salinas-Carmona, M. I. Popa, Y. Inoue, M. X. Rangaka, I. V. Lyadova, G. Curina, L. Ryan, Surender K. Sharma, M. Eyigor, T. A. Slavyanskaya, A. Zaigler, P. P. Jena, F. Kalpaklioglu, M. McAulay, N. S. Shmitova, B. López, L. Ly, T. G. D. França, Y. Kita, P. Di Carlo, K. L. Griffiths, M. Jansson, A. Brech, S. C. De Cassan, A. Bascioglu, D. Kaufmann, R. I. Sepiashvili, T. Yamamoto, D. Hayashi, Y. Sekine, F. J. Sànchez-Garcìa, C. Manca, H. McShane, H. Nakatani, Thumbi Ndung'u, A. L. Pereira-Suárez, N. Allie, D. Desjardins, F. Chiuso-Minicucci, A. T. Keyser, B. Abel, M. Kozioł-Montewka, C. K. Lee, I. Yano, A. Sonawane, K. H. Skolimowska, J. Welch, C. Park, G. Kaplan, K. Kobayashi, A. Yahagi, I. Honda, A. Y. Arce-Mendoza, K. A. Wilkinson, A. Stryhn, J. P. Christensen, W. P. J. Franken, J. A. Awuh, L. Titone, L. Fick, A. De Giuseppe, N. Yokobori, G. Griffiths, I. Sugawara, N. G. Simsek, M. Correia-Neves, M. S. Hassan, N. Caccamo, M. Hernández, R. Hernández-Pando, S. A. Im, J. Mazurek, U. Sahin, O. D. Chuquimia, H. A. Fletcher, I. Cherkaoui, E. Fick, C. Ganoza, L. L. W. Ishikawa, B. Walker, S. Akira, H. Husebye, R. El Aouad, T. Okazaki, B. Villarreal-Ramos, Y. Nishida, G. Guggino, Y. Kaneda, K. Rebe, G. G. Guerrero, G. Cangelosi, D. Clifford, O. Lund, L. Barrera, A. Hasilik, M. Seki, A. Thankappan, T. Espevik, T. Yamazaki, A. Salerno, N. N. Chegou, M. Lee, D. Fallows, W. A. Hanekom, M. Skold, S. Chetty, M. Serter, G. Matsuzaki, P. Pasquali, M. Ntsekhe, O. Cildag, N. Kanamaru, T. Nakajima, F. E. Lund, F. Dieli, C. Kishigami, Victoria O. Kasprowicz, S. Nakae, G. D. Hussey, Y. Iwakura, V. Quesniaux, H. Lee, M. Mitsuyama, C. Montagnoli, S. Cho, S. Joosten, Ø. Halaas, A. Rendon, V. J. F. Quesniaux, P. K. Saha, F. Claudio-Piedras, M. Polatli, S. Sato, Parissa Farnia, G. Gutièrrez-Iglesias, M. Soofi, A. Minassian, S. I. Grivennikov, M. Steigedal, H. Choi

Publikováno v: International Immunology. 22:iii111-iii121

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7d60777840dee643cc20d12467544ce9
https://doi.org/10.1093/intimm/dxq241

Expression cloning of a cDNA encoding a novel murine B cell activation marker. Homology to human CD38

Autor: N Harada, L Santos-Argumedo, R Chang, J C Grimaldi, F E Lund, C I Brannan, N G Copeland, N A Jenkins, A W Heath, R M Parkhouse

Publikováno v: The Journal of Immunology. 151:3111-3118

A rat mAb (NIM-R5) has recently been prepared against a novel murine B cell activation marker. We report here isolation of a cDNA (1-19) encoding the B cell-derived protein recognized by NIM-R5 antibody. This cDNA contains an open reading frame that

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1c3b53ca10c3997e922a917ba825b615
https://doi.org/10.4049/jimmunol.151.6.3111

MHC class II limits the functional expression of endogenous superantigens in B cells

Autor: F E Lund, T D Randall, D L Woodland, R B Corley

Publikováno v: The Journal of Immunology. 150:78-86

The open reading frames of the 3' long terminal repeat of mouse mammary tumor viruses (MMTV) encode superantigens. When expressed with MHC class II molecules on the surface of B cells, superantigens stimulate T cells expressing receptors with particu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a65670687afb40f260dac2d052c38563
https://doi.org/10.4049/jimmunol.150.1.78

CD38 signaling in B lymphocytes is controlled by its ectodomain but occurs independently of enzymatically generated ADP-ribose or cyclic ADP-ribose

Autor: F E, Lund, H M, Muller-Steffner, N, Yu, C D, Stout, F, Schuber, M C, Howard

Publikováno v: Journal of immunology (Baltimore, Md. : 1950). 162(5)

CD38 is a type II transmembrane glycoprotein that is expressed by many cell types including lymphocytes. Signaling through CD38 on B lymphocytes can mediate B cell activation, proliferation, and cytokine secretion. Additionally, coligation of CD38 an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::92dc043d3f9de16fefea90a8c6bbc4fa
https://pubmed.ncbi.nlm.nih.gov/10072513

Signaling through CD38 augments B cell antigen receptor (BCR) responses and is dependent on BCR expression

Autor: F E, Lund, N, Yu, K M, Kim, M, Reth, M C, Howard

Publikováno v: Journal of immunology (Baltimore, Md. : 1950). 157(4)

mAbs directed against the ectoenzyme CD38 will induce B cell proliferation in normal resting B lymphocytes, but cannot induce proliferation in B cells that are unresponsive to B cell Ag receptor (BCR) cross-linking. Using the CD38- murine B cell line

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c9c47d648bd730545d5166de39a9f240
https://pubmed.ncbi.nlm.nih.gov/8759726