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1. Full Text Systemic Increase in the Ratio between Foxp3+ and IL-17-Producing CD4+ T Cells in Healthy Pregnancy but Not in Preeclampsia
by Santner-Nanan, Brigitte and Peek, Michael John and Khanam, Roma and Richarts, Luise and Zhu, Erhua and Fazekas de St Groth, Barbara and Nanan, Ralph
The Journal of Immunology, ISSN 0022-1767, 12/2009, Volume 183, Issue 11, pp. 7023 - 7030
Preeclampsia is the leading cause of morbidity and mortality in pregnancy. Although the etiology of preeclampsia is still unclear, it is believed to involve... 
GROWTH-FACTOR-BETA | MULTIPLE-SCLEROSIS | REGULATORY CELLS | SPONTANEOUS-ABORTION | TRANSCRIPTION FACTOR FOXP3 | SOLUBLE ENDOGLIN | PERIPHERAL-BLOOD | FETAL REJECTION | IMMUNOLOGY | EXPRESSION | TH17 CELLS | Forkhead Transcription Factors - immunology | T-Lymphocyte Subsets - immunology | T-Lymphocytes, Regulatory - metabolism | Humans | Interleukin-17 - immunology | Interleukin-7 Receptor alpha Subunit - immunology | Pregnancy - immunology | T-Lymphocytes, Regulatory - immunology | CD4-Positive T-Lymphocytes - immunology | Endoglin | Flow Cytometry | Forkhead Transcription Factors - metabolism | Adult | Female | Pre-Eclampsia - metabolism | Interleukin-2 Receptor alpha Subunit - immunology | Enzyme-Linked Immunosorbent Assay | CD4-Positive T-Lymphocytes - metabolism | Receptors, Cell Surface - blood | Interleukin-17 - metabolism | Antigens, CD - blood | Interleukin-2 Receptor alpha Subunit - metabolism | T-Lymphocyte Subsets - metabolism | Interleukin-7 Receptor alpha Subunit - metabolism | Pre-Eclampsia - blood | Pre-Eclampsia - immunology | Index Medicus | Abridged Index Medicus
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2. Full Text Runx3 specifies lineage commitment of innate lymphoid cells
by Ebihara, Takashi and Song, Christina and Ryu, Stacy H and Plougastel-Douglas, Beatrice and Yang, Liping and Levanon, Ditsa and Groner, Yoram and Bern, Michael D and Stappenbeck, Thaddeus S and Colonna, Marco and Egawa, Takeshi and Yokoyama, Wayne M
Nature Immunology, ISSN 1529-2908, 10/2015, Volume 16, Issue 11, pp. 1124 - 1133
Subsets of innate lymphoid cells (ILCs) reside in the mucosa and regulate immune responses to external pathogens. While ILCs can be phenotypically classified... 
IMMUNITY | ROR-GAMMA-T | ARYL-HYDROCARBON RECEPTOR | TRANSCRIPTION FACTOR GATA3 | IFN-GAMMA | DRIVES | NOTCH | NKP46(+) CELLS | DIFFERENTIATION | IMMUNOLOGY | TISSUE INDUCER CELLS | Core Binding Factor Alpha 3 Subunit - metabolism | Core Binding Factor beta Subunit - deficiency | Citrobacter rodentium - pathogenicity | Core Binding Factor beta Subunit - genetics | Lymphocyte Subsets - immunology | Enterobacteriaceae Infections - immunology | Intestinal Mucosa - cytology | Lymphocyte Subsets - metabolism | Lymphocyte Subsets - cytology | Basic Helix-Loop-Helix Transcription Factors - metabolism | Intestinal Mucosa - immunology | Nuclear Receptor Subfamily 1, Group F, Member 3 - metabolism | Receptors, Aryl Hydrocarbon - metabolism | Antigens, Ly - metabolism | Nuclear Receptor Subfamily 1, Group F, Member 3 - deficiency | Nuclear Receptor Subfamily 1, Group F, Member 3 - genetics | Core Binding Factor beta Subunit - metabolism | Basic Helix-Loop-Helix Transcription Factors - genetics | Citrobacter rodentium - immunology | Mice, Inbred C57BL | Receptors, Aryl Hydrocarbon - genetics | Enterobacteriaceae Infections - etiology | Immunity, Innate | Mice, Knockout | Cell Differentiation - immunology | Animals | Core Binding Factor Alpha 3 Subunit - deficiency | Interleukin-7 Receptor alpha Subunit - metabolism | Core Binding Factor Alpha 3 Subunit - genetics | Natural Cytotoxicity Triggering Receptor 1 - metabolism | Mice | Cell Lineage - immunology | Physiological aspects | Genetic aspects | Immune response | Research | B cells | Index Medicus
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3. Full Text IL-2-dependent adaptive control of NK cell homeostasis
by Gasteiger, Georg and Hemmers, Saskia and Bos, Paula D and Sun, Joseph C and Rudensky, Alexander Y
Journal of Experimental Medicine, ISSN 0022-1007, 06/2013, Volume 210, Issue 6, pp. 1179 - 1187
Activation and expansion of T and B lymphocytes and myeloid cells are controlled by Foxp3(+) regulatory T cells (T reg cells), and their deficiency results in... 
INTERLEUKIN-2 | MEDICINE, RESEARCH & EXPERIMENTAL | IMMUNITY | APOPTOSIS | NATURAL-KILLER-CELLS | TGF-BETA | INCREASED SUSCEPTIBILITY | IN-VIVO | REGULATORY T-CELLS | INNATE LYMPHOID-CELLS | IMMUNOLOGY | MATURATION | Interleukin-2 - metabolism | T-Lymphocytes, Regulatory - metabolism | Mice, Inbred C57BL | CD4-Positive T-Lymphocytes - metabolism | Homeostasis - immunology | Interleukin-12 - metabolism | Interleukin-7 Receptor alpha Subunit - immunology | T-Lymphocytes, Regulatory - immunology | CD4-Positive T-Lymphocytes - immunology | Lymphocyte Activation - immunology | Animals | Interleukin-2 - immunology | Interleukin-2 Receptor alpha Subunit - metabolism | Interleukin-7 Receptor alpha Subunit - metabolism | Interleukin-12 - immunology | Killer Cells, Natural - immunology | Mice | Killer Cells, Natural - metabolism | Interleukin-2 Receptor alpha Subunit - immunology | Index Medicus
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4. Full Text Functional and genomic profiling of effector CD8 T cell subsets with distinct memory fates
by Sarkar, Surojit and Kalia, Vandana and Haining, W. Nicholas and Konieczny, Bogumila T and Subramaniam, Shruti and Ahmed, Rafi
Journal of Experimental Medicine, ISSN 0022-1007, 03/2008, Volume 205, Issue 3, pp. 625 - 640
An important question in memory development is understanding the differences between effector CD8 T cells that die versus effector cells that survive and give... 
MEDICINE, RESEARCH & EXPERIMENTAL | LINEAGE RELATIONSHIP | PROTECTIVE IMMUNITY | IMMUNOLOGICAL MEMORY | LYMPHOCYTE RESPONSES | SELECTIVE EXPRESSION | CLONAL EXPANSION | IN-VIVO | IL-7 RECEPTOR-ALPHA | IMMUNOLOGY | VIRAL-INFECTION | CUTTING EDGE | Lymphocytic choriomeningitis virus - immunology | CD8-Positive T-Lymphocytes - cytology | Receptors, Interleukin-7 - metabolism | Cell Proliferation | Oligonucleotide Array Sequence Analysis | Down-Regulation | Mice, Inbred C57BL | Mice, Transgenic | Gene Expression Profiling | CD8-Positive T-Lymphocytes - classification | Receptors, Interleukin-7 - genetics | Animals | Interleukin-7 Receptor alpha Subunit - metabolism | CD8-Positive T-Lymphocytes - metabolism | Lymphocytic choriomeningitis virus - genetics | Immunologic Memory | Cell Differentiation | Granzymes - biosynthesis | Interleukin-7 Receptor alpha Subunit - genetics | Mice | CD8-Positive T-Lymphocytes - immunology | Interleukin-2 - biosynthesis | Receptors, Immunologic - genetics | Receptors, Immunologic - metabolism | Index Medicus
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5. Full Text Activation-induced FOXP3 in human T effector cells does not suppress proliferation or cytokine production
by Allan, Sarah E and Crome, Sarah Q and Crellin, Natasha K and Passerini, Laura and Steiner, Theodore S and Bacchetta, Rosa and Roncarolo, Maria G and Levings, Megan K
International Immunology, ISSN 0953-8178, 4/2007, Volume 19, Issue 4, pp. 345 - 354
Forkhead box P3 (FOXP3) is currently thought to be the most specific marker for naturally occurring CD4+CD25+ T regulatory cells (nTregs). In mice, expression... 
INTERLEUKIN-2 | TGF-BETA | T cell activation | transcription factors | INDUCTION | IMMUNOLOGY | T cells | REGULATORY-CELLS | TRANSCRIPTION FACTOR FOXP3 | COSTIMULATION | GENERATION | FLOW-CYTOMETRY | DIFFERENTIATION | human | EXPRESSION | tolerance | T-Lymphocyte Subsets - immunology | Cysteine - analogs & derivatives | T-Lymphocytes, Regulatory - metabolism | Cell Proliferation | Coculture Techniques | Humans | Clonal Anergy | Receptors, Nerve Growth Factor - metabolism | Interferon-gamma - metabolism | Antigens, CD - metabolism | T-Lymphocytes, Regulatory - immunology | CD4-Positive T-Lymphocytes - immunology | Flagellin - pharmacology | Lymphocyte Activation - immunology | Forkhead Transcription Factors - metabolism | T-Lymphocyte Subsets - drug effects | Cysteine - pharmacology | Antigens, Differentiation - metabolism | Interleukin-2 - metabolism | Receptors, Tumor Necrosis Factor - metabolism | Cell Line | Cytokines - metabolism | Lectins, C-Type | Toll-Like Receptors - immunology | CD4-Positive T-Lymphocytes - metabolism | Glucocorticoid-Induced TNFR-Related Protein | Antigens, Differentiation, T-Lymphocyte - metabolism | CD28 Antigens - immunology | Antibodies - pharmacology | CTLA-4 Antigen | T-Lymphocytes, Regulatory - drug effects | Interleukin-2 Receptor alpha Subunit - metabolism | Lipoproteins - pharmacology | T-Lymphocyte Subsets - metabolism | Interleukin-7 Receptor alpha Subunit - metabolism | CD3 Complex - immunology | Interleukin-2 - pharmacology | CD4-Positive T-Lymphocytes - drug effects | Index Medicus
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6. Full Text TLR5 Signaling Stimulates the Innate Production of IL-17 and IL-22 by CD3(neg)CD127(+) Immune Cells in Spleen and Mucosa
by Van Maele, L and Carnoy, C and Cayet, D and Songhet, P and Dumoutier, L and Ferrero, I and Janot, L and Erard, F and Bertout, J and Leger, H and Sebbane, F and Benecke, A and Renauld, JC and Hardt, WD and Ryffel, B and Sirard, JC
JOURNAL OF IMMUNOLOGY, ISSN 0022-1767, 07/2010, Volume 185, Issue 2, pp. 1177 - 1185
In adaptive immunity, Th17 lymphocytes produce the IL-17 and IL-22 cytokines that stimulate mucosal antimicrobial defenses and tissue repair. In this study, we... 
TISSUE-INDUCER CELLS | FLAGELLIN | ROR-GAMMA-T | DENDRITIC CELLS | HOST-DEFENSE | RECEPTOR | INFECTION | DIFFERENTIATION | IMMUNOLOGY | INTESTINAL EPITHELIAL-CELLS | TH17 CELLS | Spleen - immunology | Gene Expression - drug effects | Oligonucleotide Array Sequence Analysis | Toll-Like Receptor 5 - genetics | Dendritic Cells - immunology | Interleukin-17 - immunology | Ileum - metabolism | Male | Interleukin-7 Receptor alpha Subunit - immunology | Ileum - immunology | Interleukins - metabolism | Lymphoid Tissue - immunology | Flagellin - pharmacology | Interleukins - genetics | Signal Transduction - immunology | Ileum - drug effects | Mucous Membrane - cytology | CD3 Complex - genetics | Flow Cytometry | Interleukins - immunology | Gene Expression - immunology | Dendritic Cells - drug effects | Female | Interleukin-7 Receptor alpha Subunit - genetics | Dendritic Cells - metabolism | Toll-Like Receptor 5 - metabolism | Mice, Inbred C57BL | Cells, Cultured | Interleukin-17 - genetics | Lymphoid Tissue - metabolism | Mice, Transgenic | Spleen - cytology | Mice, SCID | CD3 Complex - metabolism | Mice, Knockout | Mucous Membrane - metabolism | Toll-Like Receptor 5 - immunology | Interleukin-17 - metabolism | Lymphoid Tissue - cytology | Animals | Mucous Membrane - immunology | Spleen - metabolism | Interleukin-7 Receptor alpha Subunit - metabolism | CD3 Complex - immunology | Mice | Mice, Inbred BALB C | Index Medicus | Abridged Index Medicus | Dendritic Cells | Humans | Immunity, Mucosal | Flagellin | Mucous Membrane | Toll-Like Receptor 5 | Immunity | Antibody response | Life Sciences | Salmonella enterica | Immunology | Interleukins | Gene Deletion | Protein Structure, Quaternary | Interleukin-7 Receptor alpha Subunit | Interleukin-17 | Spleen | Caco-2 Cells | Gene Expression | Signal Transduction | Antigens, CD3 | Models, Molecular | Immunity, Innate | Ileum | Lymphoid Tissue | Human health and pathology | Infectious diseases | Complementarity Determining Regions
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7. Full Text Membrane protein GARP is a receptor for latent TGF‐β on the surface of activated human Treg
by Stockis, Julie and Colau, Didier and Coulie, Pierre G and Lucas, Sophie
European Journal of Immunology, ISSN 0014-2980, 12/2009, Volume 39, Issue 12, pp. 3315 - 3322
Human Treg and Th clones secrete the latent form of TGF‐β, in which the mature TGF‐β protein is bound to the latency‐associated peptide (LAP), and is thereby... 
TGF‐b | GARP | Treg | TGF-β | DENDRITIC CELLS | TOLERANCE | FURIN | IMMUNOLOGY | FOXP3 | TGF-beta | GROWTH-FACTOR-BETA | CONVERTASE | AUTOIMMUNITY | REGULATORY T-CELLS | EXPRESSION | CLONES | T-Lymphocytes, Regulatory - metabolism | Muromonab-CD3 - immunology | Humans | T-Lymphocytes, Regulatory - immunology | Lymphocyte Activation - immunology | Flow Cytometry | T-Lymphocytes - metabolism | T-Lymphocytes, Regulatory - cytology | Cell Membrane - metabolism | Membrane Proteins - metabolism | Latent TGF-beta Binding Proteins - metabolism | Jurkat Cells | Membrane Proteins - genetics | Cells, Cultured | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Latent TGF-beta Binding Proteins - genetics | Transforming Growth Factor beta - genetics | Interleukin-2 Receptor alpha Subunit - metabolism | T-Lymphocytes - cytology | Models, Biological | Interleukin-7 Receptor alpha Subunit - metabolism | Protein Binding | T-Lymphocytes - immunology | Transforming Growth Factor beta - metabolism | CD4 Antigens - metabolism | Index Medicus
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8. Full Text Identification of an essential cytoplasmic region of interleukin-7 receptor α subunit in B-cell development
by Kasai, Hirotake and Kuwabara, Taku and Matsui, Yukihide and Nakajima, Koichi and Kondo, Motonari
International Journal of Molecular Sciences, ISSN 1661-6596, 09/2018, Volume 19, Issue 9, p. 2522
Interleukin-7 (IL-7) is essential for lymphocyte development. To identify the functional subdomains in the cytoplasmic tail of the IL-7 receptor (IL-7R) alpha... 
B-cell development | Interleukin-7 receptor | Interleukin-7 | Signal transducer and activator of transcription 5 | SEVERE COMBINED IMMUNODEFICIENCY | STEM-CELLS | JAK KINASES | BIOCHEMISTRY & MOLECULAR BIOLOGY | signal transducer and activator of transcription 5 | TYROSINE KINASES | CYTOKINE | interleukin-7 | CHEMISTRY, MULTIDISCIPLINARY | interleukin-7 receptor | SIGNAL-TRANSDUCTION | LINEAGE COMMITMENT | IL-2 RECEPTOR | MOLECULAR-BASIS | T-CELLS | B-Lymphocytes - cytology | Cell Proliferation | Signal Transduction | Lymphocyte Activation | Cytoplasm - metabolism | Protein Transport | Interleukin-7 Receptor alpha Subunit - chemistry | Cell Differentiation - genetics | STAT5 Transcription Factor - genetics | STAT5 Transcription Factor - metabolism | Interleukin-7 Receptor alpha Subunit - metabolism | Protein Binding | Interleukin-7 Receptor alpha Subunit - genetics | Protein Interaction Domains and Motifs | Mutation | B-Lymphocytes - metabolism | Interleukin-7 - metabolism | Lymphopoiesis | Cytokines | Transcription | Interleukin | Amino acids | Chains | Stat5 protein | Progenitor cells | Hemopoiesis | Interleukin 7 | Clonal deletion | Lymphocytes B | Cells (biology) | Deletion | Identification | Kinases | Proteins | Signal transduction | Cell growth | Immunology | Stem cells | Binding sites | Index Medicus
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9. Full Text An IL-2 Paradox: Blocking CD25 on T Cells Induces IL-2-Driven Activation of CD56(bright) NK Cells
by Martin, JF and Perry, JSA and Jakhete, NR and Wang, X and Bielekova, B
JOURNAL OF IMMUNOLOGY, ISSN 0022-1767, 07/2010, Volume 185, Issue 2, pp. 1311 - 1320
Daclizumab (Dac), an Ab against the IL-2R alpha-chain, inhibits brain inflammation in patients with multiple sclerosis, while expanding CD56(bright)... 
NATURAL-KILLER-CELLS | REMITTING MULTIPLE-SCLEROSIS | IN-VIVO | DISEASE | DACLIZUMAB | RECEPTOR-ALPHA-CHAIN | ANTIBODY | PERIPHERAL-BLOOD | INTERFERON-BETA | IMMUNOLOGY | EXPRESSION | Forkhead Transcription Factors - immunology | Leukocytes, Mononuclear - metabolism | T-Lymphocytes, Regulatory - metabolism | Humans | Interleukin-7 Receptor alpha Subunit - immunology | Lewis X Antigen - metabolism | T-Lymphocytes, Regulatory - immunology | Antibodies, Monoclonal, Humanized | Signal Transduction - immunology | Flow Cytometry | Interleukin-2 - immunology | T-Lymphocytes - metabolism | Forkhead Transcription Factors - metabolism | T-Lymphocytes - drug effects | Leukocytes, Mononuclear - immunology | Immunoglobulin G - pharmacology | Killer Cells, Natural - immunology | CD56 Antigen - immunology | Cytotoxicity, Immunologic - drug effects | Immunosuppressive Agents - pharmacology | Interleukin-7 - metabolism | Interleukin-2 Receptor alpha Subunit - immunology | Interleukin-2 - metabolism | CD56 Antigen - metabolism | Cell Line | Antibodies, Monoclonal - pharmacology | Cells, Cultured | Lewis X Antigen - immunology | T-Lymphocytes, Regulatory - drug effects | Interleukin-7 - immunology | Interleukin-2 Receptor alpha Subunit - metabolism | Signal Transduction - drug effects | Interleukin-7 Receptor alpha Subunit - metabolism | Lewis X Antigen - pharmacology | K562 Cells | Interleukin-2 - pharmacology | Leukocytes, Mononuclear - cytology | T-Lymphocytes - immunology | Cell Proliferation - drug effects | Killer Cells, Natural - drug effects | Killer Cells, Natural - metabolism | Cytotoxicity, Immunologic - immunology | Index Medicus | Abridged Index Medicus
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10. Full Text The heterogeneity of human CD127+ innate lymphoid cells revealed by single-cell RNA sequencing
by Björklund, Asa K and Forkel, Marianne and Picelli, Simone and Konya, Viktoria and Theorell, Jakob and Friberg, Danielle and Sandberg, Rickard and Mjösberg, Jenny and Teknisk-naturvetenskapliga vetenskapsområdet and Biologiska sektionen and Molekylär evolution and Uppsala universitet and Institutionen för cell- och molekylärbiologi
Nature Immunology, ISSN 1529-2908, 04/2016, Volume 17, Issue 4, pp. 451 - 460
Innate lymphoid cells (ILCs) are increasingly appreciated as important participants in homeostasis and inflammation. Substantial plasticity and heterogeneity... 
NK CELLS | TRANSCRIPTOME | PACKAGE | GENE-EXPRESSION | NOTCH | T-CELL | FETAL | DIFFERENTIATION | IMMUNOLOGY | INDUCER | SEQ | Leukocytes, Mononuclear - metabolism | Humans | Middle Aged | Child, Preschool | Male | Gene Expression Profiling | Lymphocyte Subsets - immunology | Palatine Tonsil - immunology | Palatine Tonsil - cytology | Young Adult | Lymphocyte Subsets - metabolism | Flow Cytometry | Lymphocytes - immunology | Leukocytes, Mononuclear - immunology | Polymerase Chain Reaction | Killer Cells, Natural - immunology | Adult | Female | Child | Lymphocytes - metabolism | Immunity, Innate - immunology | Sequence Analysis, RNA | Interleukin-7 Receptor alpha Subunit - metabolism | Aged | Killer Cells, Natural - metabolism | Index Medicus | Basic Medicine | Immunologi inom det medicinska området | Medical and Health Sciences | Medicin och hälsovetenskap | Immunology in the medical area | Medicinska och farmaceutiska grundvetenskaper
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11. Full Text Spatial Map of Human T Cell Compartmentalization and Maintenance over Decades of Life
by Thome, Joseph J.C and Yudanin, Naomi and Ohmura, Yoshiaki and Kubota, Masaru and Grinshpun, Boris and Sathaliyawala, Taheri and Kato, Tomoaki and Lerner, Harvey and Shen, Yufeng and Farber, Donna L
Cell, ISSN 0092-8674, 11/2014, Volume 159, Issue 4, pp. 814 - 828
Mechanisms for human memory T cell differentiation and maintenance have largely been inferred from studies of peripheral blood, though the majority of T cells... 
RHEUMATOID-ARTHRITIS | EFFECTOR-MEMORY | RESIDENT | LYMPHOID ORGANS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DOWN-REGULATION | CD4(+) | SUBSETS | CCR7 | DIFFERENTIATION | EXPRESSION | CELL BIOLOGY | T-Lymphocyte Subsets - immunology | Receptors, Antigen, T-Cell - chemistry | T-Lymphocyte Subsets - cytology | Humans | Middle Aged | Child, Preschool | CD28 Antigens - metabolism | Lymphoid Tissue - immunology | Young Adult | Lymphoid Tissue - cytology | Aging - immunology | Mucous Membrane - cytology | Mucous Membrane - immunology | T-Lymphocytes - cytology | T-Lymphocytes - metabolism | T-Lymphocyte Subsets - metabolism | Interleukin-7 Receptor alpha Subunit - metabolism | Adolescent | Adult | T-Lymphocytes - immunology | Aged | Cell Differentiation | Tissue Donors | Child | Transplantation of organs, tissues, etc | Microbiology | T cells | Cell differentiation | Analysis | Genomics | Index Medicus
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12. Full Text CD45RA Distinguishes CD4+CD25+CD127−/low TSDR Demethylated Regulatory T Cell Subpopulations With Differential Stability and Susceptibility to Tacrolimus-Mediated Inhibition of Suppression
by Arroyo Hornero, Rebeca and Betts, Gareth J and Sawitzki, Birgit and Vogt, Katrin and Harden, Paul N and Wood, Kathryn J
Transplantation, ISSN 0041-1337, 02/2017, Volume 101, Issue 2, pp. 302 - 309
BACKGROUNDAdoptive transfer of forkhead box protein (FOX)3 regulatory T (Treg) cells offers a promising strategy to reduce damage to an allograft by the... 
Forkhead Transcription Factors - immunology | T-Lymphocytes, Regulatory - metabolism | Calcineurin Inhibitors - pharmacology | Leukocyte Common Antigens - metabolism | Cytokines - metabolism | Humans | Cells, Cultured | Interleukin-7 Receptor alpha Subunit - immunology | T-Lymphocytes, Regulatory - immunology | Leukocyte Common Antigens - immunology | DNA Methylation | Phenotype | T-Lymphocytes, Regulatory - drug effects | Flow Cytometry | Interleukin-2 Receptor alpha Subunit - metabolism | Forkhead Transcription Factors - metabolism | Lymphocyte Activation - drug effects | Interleukin-7 Receptor alpha Subunit - metabolism | Tacrolimus - pharmacology | Immunophenotyping - methods | Cell Proliferation - drug effects | Immunosuppressive Agents - pharmacology | Cytokines - immunology | Interleukin-2 Receptor alpha Subunit - immunology | Index Medicus | Original Basic Science—General
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13. Full Text Enhanced innate type 2 immune response in peripheral blood from patients with asthma
by Bartemes, Kathleen R., BA and Kephart, Gail M., BS and Fox, Stephanie J., MD and Kita, Hirohito, MD
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2014, Volume 134, Issue 3, pp. 671 - 678.e4
Background In mice, group 2 innate lymphoid cells (ILC2s) likely mediate helminth immunity, inflammation, and tissue repair and remodeling. However, the... 
Allergy and Immunology | ILC2 | innate immunity | IL-5 | allergy | IL-25 | asthma | IL-13 | IL-33 | HYPERREACTIVITY | POPULATION | CYTOKINES | HOMEOSTASIS | AIRWAY INFLAMMATION | IMMUNOLOGY | TRANSCRIPTION FACTOR GATA3 | ALLERGIC-ASTHMA | LYMPHOID-CELLS | ATOPIC ASTHMA | Asthma - diagnosis | Cell Separation | Rhinitis, Allergic - immunology | Humans | Middle Aged | Cells, Cultured | Male | Th2 Cells - immunology | Immunity, Innate | Receptors, Prostaglandin - metabolism | Rhinitis, Allergic - diagnosis | Flow Cytometry | Lymphocytes - immunology | Interleukin-7 Receptor alpha Subunit - metabolism | Interleukins - immunology | Asthma - immunology | Female | Cell Differentiation | Blood Circulation | Receptors, Immunologic - metabolism | Immune response | Asthma | Chlorophyll | Allergies | Immune system | Index Medicus | Abridged Index Medicus
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14. Full Text Human CD4 + CD25 + CD127 hi cells and the Th1/Th2 phenotype
by Narsale, Aditi and Moya, Rosita and Davies, Joanna Davida
Clinical immunology (Orlando, Fla.), ISSN 1521-6616, 03/2018, Volume 188, pp. 103 - 112
CD4 T cells that co-express CD25 and CD127 (CD25 CD127 ) make up around 20% of all circulating CD4 memory T cells in healthy people. The clinical significance... 
T-Lymphocyte Subsets - immunology | Cytokines - metabolism | Humans | CD4-Positive T-Lymphocytes - metabolism | Immunophenotyping | Inflammation - immunology | Interleukin-7 Receptor alpha Subunit - immunology | Th2 Cells - immunology | Th1 Cells - immunology | Th2 Cells - metabolism | CD4-Positive T-Lymphocytes - immunology | Th1 Cells - metabolism | Inflammation - metabolism | Interleukin-2 Receptor alpha Subunit - metabolism | T-Lymphocyte Subsets - metabolism | Interleukin-7 Receptor alpha Subunit - metabolism | Immunologic Memory - immunology | Cytokines - immunology | Interleukin-2 Receptor alpha Subunit - immunology
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15. Full Text Recombinant human interleukin-7 (CYT107) promotes T-cell recovery after allogeneic stem cell transplantation
by Perales, Miguel-Angel and Goldberg, Jenna D and Yuan, Jianda and Koehne, Guenther and Lechner, Lauren and Papadopoulos, Esperanza B and Young, James W and Jakubowski, Ann A and Zaidi, Bushra and Gallardo, Humilidad and Liu, Cailian and Rasalan, Teresa and Wolchok, Jedd D and Croughs, Therese and Morre, Michel and Devlin, Sean M and Van Den Brink, Marcel R. M
Blood, ISSN 0006-4971, 12/2012, Volume 120, Issue 24, pp. 4882 - 4891
Delays in immune recovery after allogeneic hematopoietic stem cell transplantation (allo-HSCT) are associated with increased risks of infection and relapse.... 
LYMPHOCYTE RECOVERY | MESSENGER-RNA | THYMIC OUTPUT | BONE-MARROW-TRANSPLANTATION | IMMUNE RECONSTITUTION | IN-VIVO | HIV-1 INFECTION | MEMORY CELLS | HEMATOLOGY | VERSUS-HOST-DISEASE | IL-7 | Hematologic Neoplasms - therapy | Recombinant Proteins - therapeutic use | Cell Proliferation | Area Under Curve | Humans | Middle Aged | Male | Metabolic Clearance Rate | Recombinant Proteins - pharmacokinetics | Interleukin-7 Receptor alpha Subunit - immunology | Recombinant Proteins - adverse effects | Transplantation, Homologous | CD4-Positive T-Lymphocytes - immunology | Dose-Response Relationship, Drug | Interleukin-7 - genetics | T-Lymphocytes - metabolism | Interleukin-7 - pharmacokinetics | T-Lymphocytes - drug effects | CD8-Positive T-Lymphocytes - metabolism | Adult | Female | Receptors, Antigen, T-Cell - immunology | Receptors, Antigen, T-Cell - metabolism | Gene Rearrangement, T-Lymphocyte | CD4-Positive T-Lymphocytes - metabolism | Treatment Outcome | Combined Modality Therapy | CD8-Positive T-Lymphocytes - drug effects | Graft vs Host Disease - chemically induced | Interleukin-7 Receptor alpha Subunit - metabolism | Interleukin-7 - therapeutic use | T-Lymphocytes - immunology | Aged | Receptors, Antigen, T-Cell - genetics | Hematologic Neoplasms - immunology | Hematopoietic Stem Cell Transplantation - methods | CD8-Positive T-Lymphocytes - immunology | CD4-Positive T-Lymphocytes - drug effects | Index Medicus | Abridged Index Medicus | Clinical Trials and Observations | Transplantation
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