Advances in Immunology, Vol. 40 - download pdf or read online

By Frank J. Dixon, K. Frank Austen, Leroy E. Hood, Jonathan W. Uhr (Eds.)

ISBN-10: 0120224402

ISBN-13: 9780120224401

Show description

Read or Download Advances in Immunology, Vol. 40 PDF

Best biology books

Download e-book for kindle: Advances in Systems Biology by Hans-Michael Kaltenbach, Jörg Stelling (auth.), Igor I.

The overseas Society for platforms Biology (ISSB) is a society geared toward advancing world-wide platforms biology learn by way of offering a discussion board for clinical discussions and diverse educational providers. The ISSB is helping coordinate researchers to shape alliances for assembly the original wishes of multidisciplinary and foreign platforms biology learn.

Elizabeth H. Harris (auth.), J. -D. Rochaix, M.'s The Molecular Biology of Chloroplasts and Mitochondria in PDF

` . .. might be steered not just to graduate scholars and researchers in photosynthesis, but in addition to these within the fields of biochemistry, molecular biology, biophysics, body structure and phycology. a lot of them will examine that Chlamydomonas is a superb version process for organic learn, and they'd use this organism of their personal learn.

Download e-book for iPad: Biology of the Antarctic Seas XIII by Louis S. Kornicker

Concerning the ProductPublished through the yankee Geophysical Union as a part of the Antarctic study sequence. content material:

Additional info for Advances in Immunology, Vol. 40

Sample text

The inclusion of either r-IL-2 or r-IFN-y instead of T cell supernatant during the initial activation with SA also resulted in enhanced subsequent responsiveness to either T cell supernatant or r-IL-2. 8 B cells were preincubated as described in the legend to Table X in the presence of various combinations of SA, T cell supernatant, 100 U/ml r-IL-2, or 100 U/ml r-IFN-y. ISC were quantitated on day 3 of the second incubation. Adapted from Jelinek et al. (1986b). 44 DIANE F. JELINEK AND PETER E. LIPSKY was somewhat less active than r-IL-2.

1983). Muraguchi and co-workers (1982) demonstrated BCGF in the MI 20,000-30,000 fraction and were able to separate this activity from IL-2. , 1983; Ambrus and Fauci, 1985). Shimizu et al. , 1985; Kishimoto, 1985). It is important to note that the high-molecular-weight human BCGF also supported differentiation. Therefore, the separation of the two BCGFs into types I and I1 provide a convenient means to distinguish the high- and low-molecularweight forms. However, a precise functional discrimination awaits further study.

Mond and colleagues (1985a) showed that r-IFN-y inhibited the murine B cell proliferative response stimulated by soluble anti-Ig antibody and could also partially suppress the induced expression of Ia. , 1985; Bich-Thuy and Fauci, 1986). Results from both of these studies also indicated that in contrast to IL-2, IFN-y alone did not support B cell growth. , 1985). , 1985). 38 DIANE F. JELINEK AND PETER E. LIPSKY Considerable controversy remains concerning the activation status of B cells responsive to IFN-y.

Download PDF sample

Advances in Immunology, Vol. 40 by Frank J. Dixon, K. Frank Austen, Leroy E. Hood, Jonathan W. Uhr (Eds.)

by Donald

Rated 4.07 of 5 – based on 34 votes