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  • 1
    Book
    Book
    Philadelphia, PA : Saunders
    Subject(s): Immunity, Cellular ; Antibody Formation immunology ; Antigens immunology ; Immune System Diseases immunology ; Lymphocytes immunology
    Type of Medium: Book
    Pages: 564 p. : , ill.
    Edition: 5th ed., updated.
    ISBN: 1416023895
    Language: English
    Note: With online acces and interactive extras (studentconsult.com)
    Location/Call number: A160 / A160:006
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  • 2
    Book
    Book
    Philadelphia : Saunders Elsevier
    Subject(s): Immunity, Cellular ; Antibody Formation immunology ; Antigens immunology ; Immune System Diseases immunology ; Lymphocytes immunology
    Type of Medium: Book
    Pages: viii, 566 p. : , ill.
    Edition: 6th ed.
    ISBN: 9781416031222
    Language: English
    Note: Properties and overview of immune responses -- Innate immunity -- Cells and tissues of the adaptive immune system -- Antibodies and antigens -- The major histocompatibility complex -- Antigen processing and presentation to T lymphocytes -- Antigen receptors and accessory molecules of T lymphocytes -- Lymphocyte development and the rearrangement and expression of antigen receptor genes -- Activation of T lymphocytes -- B cell activation and antibody production -- Immunologic tolerance -- Cytokines -- Effector mechanisms of cell-mediated immunity -- Effector mechanisms of humoral immunity -- Immunity to microbes -- Transplantation immunology -- Immunity to tumors -- Diseases caused by immune responses: hypersensitivity and autoimmunity -- Immediate hypersensitivity -- Congenital and acquired immunodeficiencies.
    Location/Call number: B060 / B060:150
    Location/Call number: B086 / B086:020
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  • 3
    Subject(s): Immunity. ; Hypersensitivity ; Immune System physiology ; Immunologic Deficiency Syndromes.
    Type of Medium: Book
    Pages: x, 335 pages : , illustrations (chiefly color) ; , 24 cm
    Edition: 5th edition.
    ISBN: 9780323390828
    Language: English
    Note: Introduction to the immune system : nomenclature, general properties, and components -- Innate immunity : the early defense against infections -- Antigen capture and presentation to lymphocytes : what lymphocytes see -- Antigen recognition in the adaptive immune system : structure of lymphocyte antigen receptors and development of immune repertoires -- T cell-mediated immunity : activation of t lymphocytes by cell-associated antigens -- Effector mechanisms of t cell-mediated immunity : functions of t cells in host defense -- Humoral immune responses : activation of b lymphocytes and production of antibodies -- Effector mechanisms of humoral immunity : elimination of extracellular microbes and toxins -- Immunological tolerance and autoimmunity : self-nonself discrimination in the immune system and its failure -- Immune responses against tumors and transplants : immunity to noninfectious transformed and foreign cells -- Hypersensitivity : disorders caused by immune responses -- Congenital and acquired immunodeficiencies : diseases caused by defective immunity.
    Location/Call number: Library / QR181:099(5)
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  • 4
    Book
    Book
    Philadelphia : Saunders Elsevier
    Subject(s): Immunity, Cellular ; Antibody Formation immunology ; Antigens immunology ; Immune System Diseases immunology ; Lymphocytes immunology
    Type of Medium: Book
    Pages: x, 565 p. : , ill.
    Edition: 9th ed.
    ISBN: 9780323479783
    Language: English
    Note: For online access to this volume please contact the library staff in room D124 (phone 3661, e-mail: http://www.dkfz.de/de/zbib/mitarbeiter/kontakt/fernleihe.php , Properties and overview of immune responses -- Innate immunity -- Cells and tissues of the adaptive immune system -- Antibodies and antigens -- The major histocompatibility complex -- Antigen processing and presentation to T lymphocytes -- Antigen receptors and accessory molecules of T lymphocytes -- Lymphocyte development and the rearrangement and expression of antigen receptor genes -- Activation of T lymphocytes -- B cell activation and antibody production -- Immunologic tolerance -- Cytokines -- Effector mechanisms of cell-mediated immunity -- Effector mechanisms of humoral immunity -- Immunity to microbes -- Transplantation immunology -- Immunity to tumors -- Diseases caused by immune responses: hypersensitivity and autoimmunity -- Immediate hypersensitivity -- Congenital and acquired immunodeficiencies.
    Location/Call number: Library / QR181:095(9)
    Location/Call number: ED01 / L401:007
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  • 5
    Subject(s): Immunity. ; Hypersensitivity ; Immune System physiology ; Immunologic Deficiency Syndromes.
    Type of Medium: Book
    Pages: v, 345 pages : , illustrations (chiefly color) ; , 24 cm
    Edition: 7th edition.
    ISBN: 9780443105197
    Language: English
    Location/Call number: Library / QR181:099(7)
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Immunological reviews 123 (1991), S. 0 
    ISSN: 1600-065X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Physiology 68 (2006), S. 67-95 
    ISSN: 0066-4278
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine , Biology
    Notes: Because of the anatomy, function, and nonregenerative nature of the myocardium, inflammation in this tissue is not well tolerated. Nevertheless, various diseases of the heart are characterized by inflammatory responses involving the effector mechanisms of innate and adaptive (lymphocyte-dependent) immunity. The innate immune response to ischemia-reperfusion injury is, by far, the most common cause of myocardial inflammation. Innate responses may have beneficial influences that preserve myocardial function in the short term but may be maladaptive in chronic states. Adaptive responses in the myocardium occur with infection or loss of tolerance, and lead to myocarditis. Given the narrow margin for benefit of cardiac inflammation, special regulatory mechanisms likely raise the threshold, compared to other tissues, for the induction and persistence of adaptive immune responses. These mechanisms include strong central and peripheral T cell tolerance to heart antigens and induction of anti-inflammatory feedback mechanisms involving cytokines such as interferon-??.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 111 (1982), S. 213-217 
    ISSN: 0021-9541
    Subject(s): Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The phenothiazine, trifluoperazine, and the mitogenic lectins, phytohemagglutinin (PHA) and Concanavalin A (Con A), were tested for their effects on human lymphocyte plasma membrane Ca-activated Mg-ATPase and ATP-dependent calcium uptake. Trifluoperazine completely inhibited Ca-uptake when present from the start of the assay at concentrations of 100 m̈M or more. When added during measurement of calcium uptake, trifluoperazine reduced the rate of vesicular calcium accumulation but was unlike the calcium ionophore, A23187, which caused a rapid release of accumulated calcium from the vesicles. Trifluoperazine also inhibited membrane vesicle Ca-ATPase activity, but this inhibition was nonspecific since the Mg-ATPase and Na, K-ATPase activities were inhibited to similar extents at the same concentration of the phenothiazine. In contrast, concentrations of PHA and Con A, which are mitogenic for lymphocytes, did not cause any change in Ca-uptake when added to suspensions of membrane vesicles. Con A had no effect and PHA had a weak inhibitory effect on Ca-ATPase activity.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 14 (1980), S. 65-75 
    ISSN: 0091-7419
    Subject(s): lymphocyte ; calcium ; phytohemagglutinin ; A23187 ; Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Calcium has been suggested as an internal second messenger when lymphocytes are stimulated by mitogens to enter the cell cycle. We have assessed the effect of 2 lymphocyte stimulants, the plant lectin phytohemagglutinin (PHA) and the calcium ionophore A23187, on human lymphocyte nucleic acid synthesis, total cell calcium content, and 4 5Ca labeling. We have used an ultrasensitive method for the measurement of total cell calcium in the same samples used for radiolabeling. Mitogenic concentrations of A23187 (∼ .25 μ mole/liter) caused an increase in both total cell calcium and 4 5Ca labeling. These increases were almost completely blocked by inhibitors of mitochondrial respiration, suggesting that the calcium increment after ionophore treatment was located in the mitochondria. In contrast, total cell calcium was not altered at optimal mitogenic PHA concentrations (0.1 μg/ml and above). However, at the minimum PHA concentrations that caused stimulation (0.025 to 0.1 μg/ml), the dose response of 4 5Ca uptake was very similar to that of DNA sysnthesis. Importantly, we could not stimulate DNA synthesis with PHA without increasing lymphocyte 4 5Ca labeling. Thus, an increase in total cell calcium is not essential for mitogenesis; however, an increase in 4 5Ca exchange is closely associated with the mitogenic effects of A23187 and PHA.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Publication Date: 2021-08-09
    Description: Classical dendritic cells (cDC) are professional antigen-presenting cells (APC) that regulate immunity and tolerance. Neutrophil-derived cells with properties of DCs (nAPC) are observed in human diseases and after culture of neutrophils with cytokines. Here we show that FcγR-mediated endocytosis of antibody-antigen complexes or an anti-FcγRIIIB-antigen conjugate converts neutrophils into nAPCs that, in contrast to those generated with cytokines alone, activate T cells to levels observed with cDCs and elicit CD8+ T cell-dependent anti-tumor immunity in mice. Single cell transcript analyses and validation studies implicate the transcription factor PU.1 in neutrophil to nAPC conversion. In humans, blood nAPC frequency in lupus patients correlates with disease. Moreover, anti-FcγRIIIB-antigen conjugate treatment induces nAPCs that can activate autologous T cells when using neutrophils from individuals with myeloid neoplasms that harbor neoantigens or those vaccinated against bacterial toxins. Thus, anti-FcγRIIIB-antigen conjugate-induced conversion of neutrophils to immunogenic nAPCs may represent a possible immunotherapy for cancer and infectious diseases.
    Electronic ISSN: 2041-1723
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General , Physics
    Published by Springer Nature
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