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1. Full Text Identification of CD8+CD25+Foxp3+ suppressive T cells in colorectal cancer tissue
by Chaput, N and Louafi, S and Bardier, A and Charlotte, F and Vaillant, J-C and Ménégaux, F and Rosenzwajg, M and Lemoine, F and Klatzmann, D and Taieb, J
Gut, ISSN 0017-5749, 04/2009, Volume 58, Issue 4, pp. 520 - 529
Background:The antitumoral immune response is one determinant of colorectal cancer (CRC) outcome. Recent work suggests that Foxp3+CD25+CD4+ regulatory T cells... 
PLASMACYTOID DENDRITIC CELLS | REGULATORY-CELLS | SURVIVAL | FOXP3 EXPRESSION | GROWTH-FACTOR-BETA | TGF-BETA | IN-VIVO | DIFFERENTIATION | INTERLEUKIN-6 | GASTROENTEROLOGY & HEPATOLOGY | OVARIAN-CARCINOMA | T-Lymphocyte Subsets - immunology | Adenocarcinoma - pathology | Cell Proliferation | Humans | Middle Aged | Male | T-Lymphocytes, Regulatory - immunology | CD4-Positive T-Lymphocytes - immunology | Lymphocyte Activation - immunology | Immune Tolerance - immunology | Aged, 80 and over | Adult | Female | Cytokines - immunology | Neoplasm Invasiveness | Adenocarcinoma - immunology | Immunophenotyping | Colorectal Neoplasms - immunology | Forkhead Transcription Factors - analysis | Lymphocyte Count | Neoplasm Proteins - analysis | Aged | Colorectal Neoplasms - pathology | Neoplasm Staging | Cytokines - biosynthesis | Lymphocytes, Tumor-Infiltrating - immunology | Care and treatment | Immune response | Lymphocytes | Colorectal cancer | Physiological aspects | Development and progression | Research | Proteins | Antigens | Cytokines | Medical prognosis | Software | Experiments | Tumors | Cell adhesion & migration | Adenocarcinoma | Life Sciences | Lymphocytes, Tumor-Infiltrating | Immunology | Neoplasm Proteins | Immunotherapy | T-Lymphocytes, Regulatory | Colorectal Neoplasms | CD4-Positive T-Lymphocytes | T-Lymphocyte Subsets | Lymphocyte Activation | Immune Tolerance | Forkhead Transcription Factors
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2. Mechanisms of leukocyte activation
by Grinstein, Sergio and Rotstein, Ori David
1990, Current topics in membranes and transport, ISBN 9780121533359, Volume 35., xviii, 628
Leucocytes | Phagocytes | Lymphocytes
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3. Suppressor cells and their factors
by Krakauer, Randall S and Clough, John D
1981, ISBN 9780849361852, 174
Suppressor cells | Lymphokines | Lymphocytes T suppresseurs
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4. Interleukins and lymphocyte activation
1982, ISBN 9788716091161, Volume 63., 209
Book
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5. Full Text Preferential Generation of Follicular B Helper T Cells from Foxp3⁺ T Cells in Gut Peyer's Patches
by Masayuki Tsuji and Noriko Komatsu and Shimpei Kawamoto and Keiichiro Suzuki and Osami Kanagawa and Tasuku Honjo and Shohei Hori and Sidonia Fagarasan
Science, ISSN 0036-8075, 3/2009, Volume 323, Issue 5920, pp. 1488 - 1492
Most of the immunoglobulin A (IgA) in the gut is generated by B cells in the germinal centers of Peyer's patches through a process that requires the presence... 
T lymphocytes | Spleen | Molecules | Peyers patches | Cytokines | B lymphocytes | Plasma cells | AIDS | Reports | Mice | Small intestine | GERMINAL CENTER FORMATION | CXC CHEMOKINE RECEPTOR-5 | POPULATION | ACTIVATION | DENDRITIC CELLS | MULTIDISCIPLINARY SCIENCES | RETINOIC-ACID | DIFFERENTIATION | INTERLEUKIN-21 | LAMINA PROPRIA | EXPRESSION | T-Lymphocyte Subsets - immunology | T-Lymphocytes, Regulatory - metabolism | Spleen - immunology | T-Lymphocyte Subsets - cytology | Dendritic Cells - immunology | Germinal Center - immunology | Gene Expression Profiling | Adoptive Transfer | T-Lymphocytes, Regulatory - immunology | CD4-Positive T-Lymphocytes - immunology | CD40 Antigens - metabolism | Forkhead Transcription Factors - metabolism | T-Lymphocytes, Helper-Inducer - immunology | T-Lymphocytes, Helper-Inducer - cytology | T-Lymphocytes, Regulatory - cytology | Cell Differentiation | Intestine, Small - immunology | T-Lymphocytes, Helper-Inducer - metabolism | Lymphocyte Activation | CD4-Positive T-Lymphocytes - cytology | Down-Regulation | CD4-Positive T-Lymphocytes - metabolism | Mice, Transgenic | Spleen - cytology | Lymph Nodes - immunology | Forkhead Transcription Factors - genetics | Lymph Nodes - cytology | Peyer's Patches - cytology | Animals | B-Lymphocytes - immunology | Intestine, Small - cytology | T-Lymphocyte Subsets - metabolism | Dendritic Cells - cytology | Immunoglobulin A, Secretory - biosynthesis | Peyer's Patches - immunology | Lymphatic system | Immunology | Cellular biology | Gene expression | Rodents
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6. Full Text PD-1+ immune cell infiltration inversely correlates with survival of operable breast cancer patients
by Sun, Shenyou and Fei, Xiaochun and Mao, Yan and Wang, Xiumin and Garfield, David H and Huang, Ou and Wang, Jinglong and Yuan, Fei and Sun, Long and Yu, Qixiang and Jin, Xiaolong and Wang, Jianhua and Shen, Kunwei
Cancer Immunology, Immunotherapy, ISSN 0340-7004, 4/2014, Volume 63, Issue 4, pp. 395 - 406
The programmed death-1 (PD-1) molecule is mainly expressed on functionally “exhausted” CD8+ T cells, dampening the host antitumor immune response. We evaluated... 
Immunology | Medicine & Public Health | Oncology | Cancer Research | Breast cancer | Immune evasion | Regulatory T cells | Cancer immunotherapy | PD-1 | APOPTOSIS | PROGNOSIS | TUMOR | RISK | ANTIBODY | IMMUNOLOGY | CHEMOTHERAPY | HEPATOCELLULAR-CARCINOMA | ONCOLOGY | IMMUNOTHERAPY | CD8(+) T-LYMPHOCYTES | B7-H1 | Carcinoma, Lobular - pathology | Follow-Up Studies | Breast Neoplasms - immunology | Humans | Middle Aged | Programmed Cell Death 1 Receptor - analysis | T-Lymphocytes, Regulatory - pathology | T-Lymphocytes, Regulatory - immunology | Antigens, Differentiation, T-Lymphocyte - analysis | Aged, 80 and over | Carcinoma, Ductal, Breast - pathology | Lymphocytes, Tumor-Infiltrating - chemistry | T-Lymphocytes, Regulatory - chemistry | Carcinoma, Lobular - immunology | CD8-Positive T-Lymphocytes - chemistry | Combined Modality Therapy | Carcinoma, Lobular - radiotherapy | T-Lymphocyte Subsets - pathology | Carcinoma, Ductal, Breast - radiotherapy | Forkhead Transcription Factors - analysis | Survival Analysis | CD8-Positive T-Lymphocytes - immunology | Lymphocytes, Tumor-Infiltrating - immunology | T-Lymphocyte Subsets - immunology | Breast Neoplasms - surgery | CD8-Positive T-Lymphocytes - pathology | Prognosis | Carcinoma, Ductal, Breast - immunology | Carcinoma, Ductal, Breast - mortality | Carcinoma, Lobular - mortality | T-Lymphocytes, Cytotoxic - pathology | T-Lymphocyte Subsets - chemistry | Mastectomy | Adult | Female | Radiotherapy, Adjuvant | T-Lymphocytes, Cytotoxic - immunology | Carcinoma, Ductal, Breast - surgery | Carcinoma, Lobular - surgery | Kaplan-Meier Estimate | Disease-Free Survival | Breast Neoplasms - radiotherapy | T-Lymphocytes, Cytotoxic - chemistry | Apoptosis - immunology | Lymphocytes, Tumor-Infiltrating - pathology | Breast Neoplasms - pathology | Lymphocyte Count | Breast Neoplasms - mortality | Aged
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7. B and T cells in immune recognition
by Loor, F and Roelants, G. E
1978, ISBN 0471994383, xviii, 504
B-Lymphocytes | Immune response | Cellular recognition | T-Lymphocytes | Lymphocytes | Immunity, Cellular
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8. Full Text Anti‐tumour immunotherapy with Vγ9Vδ2 T lymphocytes: from the bench to the bedside
by Braza, Mounia S and Klein, Bernard
British Journal of Haematology, ISSN 0007-1048, 01/2013, Volume 160, Issue 2, pp. 123 - 132
Summary Gamma delta (γδ) Τ cells are non‐conventional T lymphocyte effectors that can interact with and eradicate tumour cells. Several data demonstrate that... 
gamma delta T lymphocytes | cancer | immunotherapy | monoclonal antibodies | haematological oncology | Haematological oncology | Monoclonal antibodies | Immunotherapy | Gamma delta T lymphocytes | Cancer | T-Lymphocyte Subsets - immunology | Adjuvants, Immunologic - pharmacology | Dendritic Cells - immunology | Humans | Receptors, Antigen, T-Cell, alpha-beta - analysis | Cells, Cultured - transplantation | Receptors, Antigen, T-Cell, gamma-delta - genetics | Gene Rearrangement, delta-Chain T-Cell Antigen Receptor | Mesenchymal Stromal Cells - immunology | T-Lymphocytes, Regulatory - immunology | Neoplasms - therapy | T-Lymphocytes, Cytotoxic - transplantation | T-Lymphocyte Subsets - chemistry | Diphosphonates - therapeutic use | Killer Cells, Natural - immunology | Cells, Cultured - immunology | Tumor Escape - immunology | Adaptive Immunity | T-Lymphocytes, Cytotoxic - immunology | Cells, Cultured - drug effects | Immunotherapy, Adoptive | Antigens, Neoplasm - immunology | Translational Medical Research | Clinical Trials as Topic | Immunity, Innate | T-Lymphocyte Subsets - transplantation | Immunologic Surveillance - immunology | Gene Rearrangement, gamma-Chain T-Cell Antigen Receptor | T-Lymphocytes, Cytotoxic - chemistry | Receptors, Antigen, T-Cell, gamma-delta - analysis | Neoplasms - immunology | CD8-Positive T-Lymphocytes - immunology | Dendritic Cells - transplantation | Diphosphonates - pharmacology | Immunologic Surveillance | Tumor Escape | Killer Cells, Natural | Dendritic Cells | T-Lymphocytes, Cytotoxic | Neoplasms | CD8-Positive T-Lymphocytes | Life Sciences | Immunology | Mesenchymal Stromal Cells | Receptors, Antigen, T-Cell, alpha-beta | T-Lymphocytes, Regulatory | T-Lymphocyte Subsets | Antigens, Neoplasm | Adjuvants, Immunologic | Cells, Cultured | Diphosphonates | Receptors, Antigen, T-Cell, gamma-delta
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9. Full Text Heterogeneity of Natural Foxp3⁺ T Cells: A Committed Regulatory T-Cell Lineage and an Uncommitted Minor Population Retaining Plasticity
by Noriko Komatsu and Maria Encarnita Mariotti-Ferrandiz and Ying Wang and Bernard Malissen and Herman Waldmann and Shohei Hori and Michael J. Bevan
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2009, Volume 106, Issue 6, pp. 1903 - 1908
Natural regulatory T cells (${\rm{T}}_{{\rm{reg}}} $) represent a distinct lineage of T lymphocytes committed to suppressive functions, and expression of the... 
T lymphocytes | Phenotypes | Cytokines | Spleen cells | B lymphocytes | Cell division | Mice | Down regulation | Transponders | T cell antigen receptors | Transcription factor | Lineage commitment | Immunological tolerance | transcription factor | PROGRAMS | TOLERANCE | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION FACTOR FOXP3 | lineage commitment | EXPRESSION | immunological tolerance | Mice, Inbred C57BL | Adoptive Transfer | Cell Lineage | Transforming Growth Factor beta - pharmacology | Animals | Lymphocyte Subsets - cytology | Forkhead Transcription Factors - analysis | T-Lymphocytes, Helper-Inducer - cytology | T-Lymphocytes, Regulatory - cytology | Cell Differentiation | T-Lymphocytes, Regulatory - transplantation | T-Lymphocytes, Regulatory - chemistry | Cytokines - pharmacology | T-Lymphocytes, Helper-Inducer | Life Sciences | Immunology | Lymphocyte Subsets | T-Lymphocytes, Regulatory | Forkhead Transcription Factors | Transforming Growth Factor beta | Biological Sciences
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10. Full Text Single-Cell Mass Cytometry of Differential Immune and Drug Responses Across a Human Hematopoietic Continuum
by Sean C. Bendall and Erin F. Simonds and Peng Qiu and El-ad D. Amir and Peter O. Krutzik and Rachel Finck and Robert V. Bruggner and Rachel Melamed and Angelica Trejo and Olga I. Ornatsky and Robert S. Balderas and Sylvia K. Plevritis and Karen Sachs and Dana Pe'er and Scott D. Tanner and Garry P. Nolan
Science, ISSN 0036-8075, 5/2011, Volume 332, Issue 6030, pp. 687 - 696
Flow cytometry is an essential tool for dissecting the functional complexity of hematopoiesis. We used single-cell "mass cytometry" to examine healthy human... 
T lymphocytes | Cytometry | Phosphorylation | RESEARCH ARTICLE | B lymphocytes | Stem cells | Cell lines | Bone marrow | Bone marrow cells | Cells | Hematopoietic stem cells | STEM-CELLS | ACTIVATION | LYMPHOCYTE | MULTIDISCIPLINARY SCIENCES | MYELOGENOUS LEUKEMIA | TYROSINE KINASE INHIBITOR | FLOW-CYTOMETRY | DASATINIB | IDENTIFICATION | QUANTITATIVE-ANALYSIS | SIGNALING NETWORKS | Lanthanoid Series Elements | Leukocytes, Mononuclear - metabolism | Flow Cytometry - methods | Humans | Antibodies | Lymphocyte Subsets - immunology | Lymphocyte Subsets - metabolism | T-Lymphocytes - metabolism | Hematopoiesis | Single-Cell Analysis - methods | T-Lymphocytes - drug effects | Bone Marrow Cells - immunology | Leukocytes, Mononuclear - immunology | Mass Spectrometry | Bone Marrow Cells - drug effects | B-Lymphocytes - metabolism | Dasatinib | Leukocytes, Mononuclear - drug effects | Cytokines - metabolism | Bone Marrow Cells - cytology | Lymphocyte Activation | Lymphocyte Subsets - drug effects | Immunophenotyping | Pyrimidines - pharmacology | Transition Elements | B-Lymphocytes - drug effects | Algorithms | B-Lymphocytes - immunology | Signal Transduction - drug effects | T-Lymphocytes - immunology | Protein Kinase Inhibitors - pharmacology | Thiazoles - pharmacology | Antigens, Surface - analysis | Bone Marrow Cells - metabolism | Protein-Tyrosine Kinases - antagonists & inhibitors | Evaluation | Flow cytometry | Immune response | Research | Immunopharmacology | Methods
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11. Full Text Tumor-derived exosomes regulate expression of immune function-related genes in human T cell subsets
by Muller, Laurent and Mitsuhashi, Masato and Simms, Patricia and Gooding, William E and Whiteside, Theresa L
Scientific Reports, ISSN 2045-2322, 02/2016, Volume 6, Issue 1, p. 20254
Tumor cell-derived exosomes (TEX) suppress functions of immune cells. Here, changes in the gene profiles of primary human T lymphocytes exposed in vitro to... 
MESSENGER-RNAS | CANCER-PATIENTS | EXTRACELLULAR VESICLES | MICROENVIRONMENT | MULTIDISCIPLINARY SCIENCES | MICROVESICLES | DIAGNOSTIC BIOMARKERS | INDUCE APOPTOSIS | OVARIAN-CANCER | MODULATION | LYMPHOCYTES | Exosomes - metabolism | Neoplasms - metabolism | CD8-Positive T-Lymphocytes - cytology | T-Lymphocytes, Regulatory - metabolism | T-Lymphocyte Subsets - cytology | Humans | Culture Media, Conditioned - pharmacology | RNA, Messenger - metabolism | Antigens, CD - metabolism | Lectins, C-Type - metabolism | T-Lymphocyte Subsets - drug effects | T-Lymphocytes, Regulatory - cytology | CD8-Positive T-Lymphocytes - metabolism | Real-Time Polymerase Chain Reaction | Microscopy, Electron, Transmission | CD4-Positive T-Lymphocytes - cytology | Apyrase - metabolism | CD4-Positive T-Lymphocytes - metabolism | Cells, Cultured | Antigens, Differentiation, T-Lymphocyte - metabolism | Down-Regulation - drug effects | Up-Regulation - drug effects | T-Lymphocytes, Regulatory - drug effects | T-Lymphocyte Subsets - metabolism | CD8-Positive T-Lymphocytes - drug effects | Adenosine - metabolism | Neoplasms - pathology | CD4-Positive T-Lymphocytes - drug effects | Microscopy, Fluorescence | Adenosine | Dendritic cells | CD8 antigen | Gene regulation | Data processing | T cell receptors | Lymphocytes T | Gene expression | Exosomes | Cell surface | CD4 antigen | Polymerase chain reaction | CD69 antigen | Cell activation | Lymphocytes | Down-regulation | Peripheral blood
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12. Full Text IL‐9 promotes the survival and function of human melanoma‐infiltrating CD4+CD8+ double‐positive T cells
by Parrot, Tiphaine and Allard, Mathilde and Oger, Romain and Benlalam, Houssem and Raingeard de la Blétière, Diane and Coutolleau, Anne and Preisser, Laurence and Desfrançois, Juliette and Khammari, Amir and Dréno, Brigitte and Labarrière, Nathalie and Delneste, Yves and Guardiola, Philippe and Gervois, Nadine
European Journal of Immunology, ISSN 0014-2980, 07/2016, Volume 46, Issue 7, pp. 1770 - 1782
We previously demonstrated an accumulation of tumor‐reactive CD4+CD8+ double positive (DP) T cells within melanoma‐infiltrating lymphocytes, supporting their... 
IL‐9R | IL‐9 | CD4+CD8+ double‐positive T lymphocyte | TIL | Melanoma | CD4 | IL-9R | CD8 | double-positive T lymphocyte | IL-9 | TH9 CELLS | CD8(+) | INDUCED APOPTOSIS | INTERLEUKIN-9 | RECEPTOR | PERIPHERAL-BLOOD | IMMUNOLOGY | CYTOKINE EXPRESSION | IN-VIVO | CD4(+) CD8(+) double-positive T lymphocyte | GROWTH-FACTOR | LYMPHOCYTES | T-Lymphocyte Subsets - immunology | Apoptosis - drug effects | Humans | CD4-Positive T-Lymphocytes - immunology | Lymphocyte Activation - immunology | Interleukin-9 - pharmacology | Melanoma - genetics | T-Lymphocyte Subsets - drug effects | CD8-Positive T-Lymphocytes - metabolism | Lymphocytes, Tumor-Infiltrating - metabolism | Cytotoxicity, Immunologic - drug effects | Melanoma - metabolism | Receptors, Interleukin-9 - metabolism | Gene Expression | Cytokines - metabolism | CD4-Positive T-Lymphocytes - metabolism | Cells, Cultured | Lymphocytes, Tumor-Infiltrating - drug effects | Melanoma - pathology | Cell Survival - immunology | Apoptosis - immunology | Receptors, Interleukin-9 - genetics | Lymphocyte Activation - drug effects | Melanoma - immunology | T-Lymphocyte Subsets - metabolism | CD8-Positive T-Lymphocytes - drug effects | CD8-Positive T-Lymphocytes - immunology | Interleukin-9 - immunology | CD4-Positive T-Lymphocytes - drug effects | Lymphocytes, Tumor-Infiltrating - immunology | Parrots | T cells | Tumors | Life Sciences | Cancer
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