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Books on the topic 'Humoral and cellular immunity'

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Author: Grafiati
Published: 12 June 2021
Last updated: 3 February 2022

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1

Federation of Immunological Societies of Asia-Oceania. Congress. 2nd Congress of the Federation of Immunological Societies of Asia-Oceania: Bangkok, Thailand, January 23-27, 2000. Edited by Sirisinha Stitaya, Chaiyaroj Sansanee C, and Tapchaisri Pramuan. Bologna, Italy: Monduzzi Editore, International Proceedings Division, 2000.

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2

Goss, John A. The thymus: Regulator of cellular immunity. Austin: R.G. Landes Co., 1993.

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3

Hašek, Milan. Buněčné a molekulární základy specifické imunity. Praha: Academia, 1988.

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4

Austyn, Jonathan M. Principles of cellular and molecular immunology. Oxford: Oxford University Press, 1993.

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5

International, Symposium on Cellular Immunotherapy of Cancer (1986 Racine Wis ). Cellular immunotherapy of cancer: Proceedings of the International Symposium on Cellular Immunotherapy of Cancer, held at Racine, Wisconsin, October 30-November 1, 1986. New York: Liss, 1987.

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6

International Symposium on Cellular Immunotherapy of Cancer (1986 Racine, Wis.). Cellular immunotherapy of cancer: Proceedings of the International Symposium on Cellular Immunotherapy of Cancer, held at Racine, Wisconsin, October 30-November 1, 1986. Edited by Truitt Robert L. ed, Gale Robert Peter ed, and Bortin Mortimer M. ed. New York: Liss, 1987.

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7

International, Symposium on Cellular Immunotherapy of Cancer (1986 Racine Wis ). Cellular immunotherapy of cancer: Proceedings of the International Symposium on Cellular Immunotherapy of Cancer, held at Racine, Wisconsin, Oct. 30 - Nov. 1, 1986. New York: Liss, 1987.

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8

Abbas, Abul K. Cellular and molecular immunology. 7th ed. Philadelphia: Elsevier/Saunders, 2012.

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9

NATO Advanced Research Workshop on Cellular and Humoral Immunological Components of Cerebrospinal Fluid in Multiple Sclerosis (1986 Engelhoef, Belgium). Cellular and humoral immunological components of cerebrospinal fluid in multiple sclerosis. New York: Plenum Press, 1987.

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10

Lowenthal, A., and J. Raus, eds. Cellular and Humoral Immunological Components of Cerebrospinal Fluid in Multiple Sclerosis. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4899-5348-3.

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11

International Lymphokine Workshop ((4th 1984 Schloss Elmau). Cellular and molecular biology of lymphokines: Proceedings of the Fourth International Lymphokine Workshop. Edited by Sorg Clemens, Schimpl Anneliese, and Landy Maurice. Orlando: Academic Press, 1985.

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12

CNR/EURAGE/NIH Symposium on "New Trends in Aging Research" (1985 Bologna, Italy). Immunoregulation in aging: Proceedings of the CNR/EURAGE/NIH Symposium on "New Trends in Aging Research," Bologna, Italy, November 6-9, 1985. Edited by Facchini A, Haaijman J. J, Labò G, Consiglio nazionale delle ricerche (Italy), EURAGE (Program), and National Institutes of Health (U.S.). Rijswijk: EURAGE, 1986.

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13

Michaud, Ellen. Prevention magazine's 30-day immune power program: How to strengthen your cellular defense system and resist disease. Edited by Feinstein Alice and Michaud Ellen. Emmaus, Pa: Rodale Press, 1992.

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14

Balkwill, Frances R. Cell wars. Minneapolis: Carolrhoda Books, 1993.

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15

Balkwill, Frances R. Cell wars. London: HarperCollins, 1990.

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16

Abbas, Abul K. Cellular and molecular immunology. 2nd ed. Philadelphia: W.B. Saunders, 1994.

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17

Abbas, Abul K. Cellular and molecular immunology. 6th ed. Philadelphia: Saunders Elsevier, 2007.

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18

Abbas, Abul K. Cellular and molecular immunology. 5th ed. Philadelphia, PA: Saunders, 2005.

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19

Abbas, Abul K. Cellular and molecular immunology. 3rd ed. Philadelphia: Saunders, 1997.

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20

Abbas, Abul K. Cellular and molecular immunology. 6th ed. Philadelphia: Saunders/Elsevier, 2010.

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21

Abbas, Abul K. Cellular and molecular immunology. Philadelphia: Saunders, 1991.

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22

Balkwill, Frances R. Bing jun sha shou =: Germ zappers. 8th ed. Taibei Shi: Tian xia yuan jian chu ban gu fen you xian gong si, 2004.

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23

Nobel, Symposium (68th 1987 Marstrand Sweden). Mucosal immunobiology: Cellular-molecular interactions in the mucosal immune system. Basel: Karger, 1988.

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24

Hassan, Jubril Olugbenga. Some aspects of humoral and cellular immune response to 'Salmonella typhimurium' in chickens. Birmingham: University of Birmingham, 1989.

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25

Lane, Jonathan David. Autophagy: Molecules and mechanisms. London: Portland Press Limited, 2013.

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26

Valanne, Susanna, Dan Hultmark, and Laura Vesala, eds. Recent Advances in Drosophila Cellular and Humoral Innate Immunity. Frontiers Media SA, 2020. http://dx.doi.org/10.3389/978-2-88966-191-6.

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27

A, Sacher Ronald, and American Association of Blood Banks., eds. Cellular and humoral immunotherapy and apheresis. Arlington, Va: American Association of Blood Banks, 1991.

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28

M, Snapper Clifford, ed. Cytokine regulation of humoral immunity: Basic and clinical aspects. Chichester: J. Wiley, 1996.

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29

Snapper, Clifford M. Cytokine Regulation of Humoral Immunity: Basic and Clinical Aspects. Wiley & Sons, Incorporated, John, 2008.

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30

Snapper, Clifford M. Cytokine Regulation of Humoral Immunity: Basic and Clinical Aspects. Wiley, 1996.

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31

Aging and the immune response: Cellular and humoral aspects. New York: Dekker, 1987.

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32

Raghavan, Sri. Infection in the Cancer Patient. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199976805.003.0054.

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Abstract:
Cancer patients have increased susceptibility to a variety of both common and atypical infections due to the steady increase in outpatient chemotherapy regimens, these patients are presenting more often to the emergency department when acutely ill. Already immunocompromised, patients’ chemotherapy regimens lead to neutropenia, deficits in cellular and humoral immunity, and disruption of mucosal barriers that predisposing them to severe disease presentations with high morbidity and mortality rates. There are different subsets of oncologic patients predisposed to specific infections. One of the most common presentations of oncologic chemotherapy patients is neutropenic fever caused by bacterial infection; neutropenic patients are also highly susceptible to fungal infections. Patients with hematologic malignancies, particularly those undergoing chemotherapy or bone marrow transplant, can present with inflammation of the cecum with high risk for bacterial translocation and possible perforation. Patients who have indwelling catheters or mediports are at risk for catheter-associated bloodstream infections.
33

Karcher, D. Humoral Immunity in Neurological Diseases. Springer, 2012.

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34

Remuzzi, G., S. Chiaramonte, N. Perico, and C. Ronco, eds. Humoral Immunity in Kidney Transplantation. S. Karger AG, 2008. http://dx.doi.org/10.1159/isbn.978-3-8055-8959-8.

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35

Karcher, D. Humoral Immunity in Neurological Diseases. Springer, 2014.

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36

1928-, Gupta A. P., ed. Hemocytic and humoral immunity in arthropods. New York: Wiley, 1986.

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37

Sacher, R. A., D. B. Brubaker, D. O. Kasprisin, and L. J. McCarthy. Cellular and Humoral Immunotherapy and Apheresis. S Karger Ag, 1992.

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38

Wolstenholme, G. E. W., and Maeve O'Connor. Cellular Aspects of Immunity. Wiley & Sons, Incorporated, John, 2009.

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39

Gadebusch, Hans H. Phagocytes and Cellular Immunity. Taylor & Francis Group, 2020.

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40

Gadebusch, Hans H., ed. Phagocytes and Cellular Immunity. CRC Press, 2020. http://dx.doi.org/10.1201/9780429276576.

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41

Gadebusch, Hans H. Phagocytes and Cellular Immunity. Taylor & Francis Group, 2020.

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42

E, Sim, ed. Humoral factors. Oxford: IRL Press at Oxford University Press, 1993.

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43

Pathogen subversion of cellular immunity. Copenhagen: Munksgaard, 1999.

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44

MBBS, Abul K. Abbas, Andrew H. Lichtman MD PhD, and Shiv Pillai MBBS PhD. Cellular and Molecular Immunology. Elsevier, 2017.

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45

Takeshi, Yoshida, ed. Investigation of cell-mediated immunity. Edinburgh [Lothian]: Churchill Livingstone, 1985.

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46

Cellular immunity and immunotherapy of cancer. Philadelphia, Pa: American Association for Cancer Research, 2001.

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47

Potter, M., Joost J. Oppenheim, and D. L. Rosenstreich. Cellular Functions in Immunity and Inflammation. Elsevier Science, 1985.

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48

Lichtman, Andrew H., Jordan S. Pober, and Abul K. Abbas. Cellular and Molecular Immunology. 4th ed. W.B. Saunders Company, 2000.

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49

Vaheri, Antti, James N. Mills, Christina F. Spiropoulou, and Brian Hjelle. Hantaviruses. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198570028.003.0035.

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Abstract:
Hantaviruses (genus Hantavirus, family Bunyaviridae) are rodent- and insectivore-borne zoonotic viruses. Several hantaviruses are human pathogens, some with 10-35% mortality, and cause two diseases: hemorrhagic fever with renal syndrome (HFRS) in Eurasia, and hantavirus cardiopulmonary syndrome (HCPS) in the Americas. Hantaviruses are enveloped and have a three-segmented, single-stranded, negative-sense RNA genome. The L gene encodes an RNA-dependent RNA polymerase, the M gene encodes two glycoproteins (Gn and Gc), and the S gene encodes a nucleocapsid protein. In addition, the S genes of some hantaviruses have an NSs open reading frame that can act as an interferon antagonist. Similarities between phylogenies have suggested ancient codivergence of the viruses and their hosts to many authors, but increasing evidence for frequent, recent host switching and local adaptation has led to questioning of this model. Infected rodents establish persistent infections with little or no effect on the host. Humans are infected from aerosols of rodent excreta, direct contact of broken skin or mucous membranes with infectious virus, or rodent bite. One hantavirus, Andes virus, is unique in that it is known to be transmitted from person-to-person. HFRS and HCPS, although primarily affecting kidneys and lungs, respectively, share a number of clinical features, such as capillary leakage, TNF-, and thrombocytopenia; notably, hemorrhages and alterations in renal function also occur in HCPS and cardiac and pulmonary involvement are not rare in HFRS. Of the four structural proteins, both in humoral and cellular immunity, the nucleocapsid protein appears to be the principal immunogen. Cytotoxic T-lymphocyte responses are seen in both HFRS and HCPS and may be important for both protective immunity and pathogenesis. Diagnosis is mainly based on detection of IgM antibodies although viral RNA (vRNA) may be readily, although not invariably, detected in blood, urine and saliva. For sero/genotyping neutralization tests/RNA sequencing are required. Formalin-inactivated vaccines have been widely used in China and Korea but not outside Asia. Hantaviruses are prime examples of emerging and re-emerging infections and, given the limited number of rodents and insectivores thus far studied, it is likely that many new hantaviruses will be detected in the near future.
50

Giuseppe, Remuzzi, ed. Humoral immunity in kidney transplantation: What clinicians need to know. Basel: Karger, 2009.

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