"Lymphocyte Subsets" - Books

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Select item 14152801.

Madame Curie Bioscience Database [Internet].

Austin (TX): Landes Bioscience; 2000-2013.

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Select item 14589842.

GeneReviews® [Internet].

Adam MP, Bick S, Mirzaa GM, et al., editors.

Seattle (WA): University of Washington, Seattle; 1993-2025.

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Select item 44036683.

StatPearls [Internet].

Treasure Island (FL): StatPearls Publishing; 2025 Jan-.

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Select item 16541064.

Immunobiology: The Immune System in Health and Disease. 5th edition.

Janeway CA Jr, Travers P, Walport M, et al.

New York: Garland Science; 2001.

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Select item 44650645.

Autoimmunity: From Bench to Bedside [Internet].

Anaya JM, Shoenfeld Y, Rojas-Villarraga A, et al., editors.

Bogota (Colombia): El Rosario University Press; 2013 Jul 18.

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Select item 16686906.

Holland-Frei Cancer Medicine. 6th edition.

Kufe DW, Pollock RE, Weichselbaum RR, et al., editors.

Hamilton (ON): BC Decker; 2003.

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Select item 32314347.

Military Strategies for Sustainment of Nutrition and Immune Function in the Field.

Institute of Medicine (US) Committee on Military Nutrition Research.

Washington (DC): National Academies Press (US); 1999.

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Select item 34012948.

Endotext [Internet].

Feingold KR, Ahmed SF, Anawalt B, et al., editors.

South Dartmouth (MA): MDText.com, Inc.; 2000-.

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Select item 28215249.

PDQ Cancer Information Summaries [Internet].

Bethesda (MD): National Cancer Institute (US); 2002-.

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Select item 575295010.

IRIS Toxicological Review of Formaldehyde (Inhalation) CASRN 50-00-0.

Kraft A, Bateson TF, Glenn B, et al.

Washington (DC): U.S. Environmental Protection Agency; 2024 Aug.

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Select item 568529611.

The EBMT Handbook: Hematopoietic Cell Transplantation and Cellular Therapies [Internet]. 8th edition.

Sureda A, Corbacioglu S, Greco R, et al., editors.

Cham (CH): Springer; 2024.

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Select item 236397412.

Human Herpesviruses: Biology, Therapy, and Immunoprophylaxis.

Arvin A, Campadelli-Fiume G, Mocarski E, et al., editors.

Cambridge: Cambridge University Press; 2007.

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Select item 464581013.

Signaling Mechanisms Regulating T Cell Diversity and Function.

Soboloff J, Kappes DJ, editors.

Boca Raton (FL): CRC Press/Taylor & Francis; 2018.

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Select item 424012014.

Veterans and Agent Orange: Update 2014.

Committee to Review the Health Effects in Vietnam Veterans of Exposure to Herbicides (Tenth Biennial Update); Board on the Health of Select Populations; Institute of Medicine; National Academies of Sciences, Engineering, and Medicine.

Washington (DC): National Academies Press (US); 2016 Mar 29.

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Select item 448427015.

Multiple Sclerosis: Perspectives in Treatment and Pathogenesis [Internet].

Zagon IS, McLaughlin PJ, editors.

Brisbane (AU): Codon Publications; 2017 Nov 27.

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Select item 559346216.

Toxicological Profile for Chlorinated Dibenzo-p-Dioxins.

Atlanta (GA): Agency for Toxic Substances and Disease Registry (US); 1998 Dec.

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Select item 168684017.

Retroviruses.

Coffin JM, Hughes SH, Varmus HE, editors.

Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press; 1997.

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Select item 542965418.

Toxicological Profile for Polychlorinated Biphenyls (PCBs).

Atlanta (GA): Agency for Toxic Substances and Disease Registry (US); 2000 Nov.

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Select item 316766219.

Immunodeficient Rodents: A Guide to Their Immunobiology, Husbandry, and Use.

National Research Council (US) Committee on Immunologically Compromised Rodents.

Washington (DC): National Academies Press (US); 1989.

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Select item 330226820.

Review of the Formaldehyde Assessment in the National Toxicology Program 12th Report on Carcinogens.

Committee to Review the Formaldehyde Assessment in the National Toxicology Program 12th Report on Carcinogens; Board on Environmental Studies and Toxicology; Division on Earth and Life Sciences; National Research Council.

Washington (DC): National Academies Press (US); 2014 Sep 8.

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Figure 9

Changes in the phenotype of lymphocytes recovered from M40403 treated LAK cultures. Flow cytometric analysis of lymphocyte subsets derived from splenocytes (10⁶/ml) incubated with 6000 IU IL-2/ml for 3 days with or without 10 μM M40403 (expressed as absolute cell recovery, mean ± SD). NK-1 and peanut lectin (PNA, recognizes asialo-GM-1 glycan structure) are markers for NK subsets, while Mac-1 (CD11b) is a macrophage marker.

Evaluation of a Superoxide Dismutase Mimetic As an Adjunct to Interleukin 2 Based Cancer Therapy.

Madame Curie Bioscience Database [Internet]. Austin (TX): Landes Bioscience; 2000-2013.
FIGURE WO-14

The continuum of microbial states and immune responses: a dynamic equilibrium. Microbes, including members of the symbiotic microbiota, are not inherently mutualistic or pathogen, but navigate between shades of mutualism and parasitism. Facing the microbes, the immune system is not designed to discriminate between mutualists or pathogens, but merely to react to signals, including MAMPs and antigens (Ags). The nature of the immune response is not purely regulatory or inflammatory, but more generally adjusts to the nature of the trigger it faces, like a spring that is pulled by the intensity of the microbial challenge. Furthermore, the immune system has the capacity to evolve when challenged, through generation of different types of lymphocyte subsets such as Th1, Th2, Th17, Treg, Th22 cells, and follicular T helper cells, and generation of memory lymphocytes and lymphoid tissues. This adds another level of adaptability to the immune system and provides it with the necessary flexibility to maintain homeostasis of the superorganism.
NOTE: MAMPs, microbe-associated molecular patterns.
SOURCE: Eberl (2010).

Workshop Overview.

Forum on Microbial Health; Board on Global Health; Institute of Medicine. Microbial Ecology in States of Health and Disease: Workshop Summary. Washington (DC): National Academies Press (US); 2014 Feb 18.
FIGURE A8-3

The continuum of microbial states and immune responses: a dynamic equilibrium. Microbes, including members of the symbiotic microbiota, are not inherently mutualistic or pathogen, but navigate between shades of mutualism and parasitism. Facing the microbes, the immune system is not designed to discriminate between mutualist or pathogens, but merely to react to signals, including MAMPs and antigens. The nature of the immune response is not purely regulatory or inflammatory, but more generally adjusts to the nature of the trigger it faces, like a spring that is pulled by the intensity of the microbial challenge. Furthermore, the immune system has the capacity to evolve when challenged, through generation of different types of lymphocyte subsets such as Th1, Th2, Th17, Treg, Th22 cells (Weaver et al., 2007), and follicular T helper cells (Nurieva et al., 2008), and generation of memory lymphocytes and lymphoid tissues (Round and Mazmanian, 2009). This adds another level of adaptability to the immune system and provides it with the necessary flexibility to maintain homeostasis of the superorganism. MAMP, microbe-associated molecular pattern.

Contributed Manuscripts.

Forum on Microbial Health; Board on Global Health; Institute of Medicine. Microbial Ecology in States of Health and Disease: Workshop Summary. Washington (DC): National Academies Press (US); 2014 Feb 18.