review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | U H von Andrian | |
J R Mora | |||
P2860 | cites work | Identification of a novel chemokine (CCL28), which binds CCR10 (GPR2) | Q22253984 |
Impaired IgA class switching in APRIL-deficient mice | Q24313032 | ||
CCR10 expression is a common feature of circulating and mucosal epithelial tissue IgA Ab-secreting cells | Q24684754 | ||
A novel chemokine ligand for CCR10 and CCR3 expressed by epithelial cells in mucosal tissues | Q28137982 | ||
A common mucosal chemokine (mucosae-associated epithelial chemokine/CCL28) selectively attracts IgA plasmablasts | Q28184989 | ||
DCs induce CD40-independent immunoglobulin class switching through BLyS and APRIL | Q28216755 | ||
CXCL13 is required for B1 cell homing, natural antibody production, and body cavity immunity | Q28217241 | ||
Redundant role of chemokines CCL25/TECK and CCL28/MEC in IgA+ plasmablast recruitment to the intestinal lamina propria after rotavirus infection | Q28238004 | ||
TACI is mutant in common variable immunodeficiency and IgA deficiency | Q28260786 | ||
CCL28 controls immunoglobulin (Ig)A plasma cell accumulation in the lactating mammary gland and IgA antibody transfer to the neonate | Q28283431 | ||
Class switch recombination and hypermutation require activation-induced cytidine deaminase (AID), a potential RNA editing enzyme | Q29547201 | ||
A functionally specialized population of mucosal CD103+ DCs induces Foxp3+ regulatory T cells via a TGF-beta and retinoic acid-dependent mechanism | Q29614266 | ||
In vivo depletion of CD11c+ dendritic cells abrogates priming of CD8+ T cells by exogenous cell-associated antigens | Q29615098 | ||
Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid | Q29615586 | ||
Retinoic acid imprints gut-homing specificity on T cells | Q29619126 | ||
Reciprocal TH17 and regulatory T cell differentiation mediated by retinoic acid | Q29619479 | ||
Selectins in T-cell recruitment to non-lymphoid tissues and sites of inflammation | Q30433441 | ||
Protective intestinal anti-rotavirus B cell immunity is dependent on alpha 4 beta 7 integrin expression but does not require IgA antibody production | Q31838600 | ||
Rapid acquisition of tissue-specific homing phenotypes by CD4(+) T cells activated in cutaneous or mucosal lymphoid tissues | Q33183256 | ||
Selective generation of gut tropic T cells in gut-associated lymphoid tissue (GALT): requirement for GALT dendritic cells and adjuvant. | Q33188469 | ||
Regulation of intestinal epithelial cell growth by transforming growth factor type beta | Q33840554 | ||
A primitive T cell-independent mechanism of intestinal mucosal IgA responses to commensal bacteria | Q73919528 | ||
Regulation of the T-independent humoral response by TACI | Q73923479 | ||
The regulatory effects of all-trans-retinoic acid on isotype switching: retinoic acid induces IgA switch rearrangement in cooperation with IL-5 and inhibits IgG1 switching | Q74583047 | ||
IgVH gene analysis suggests that peritoneal B cells do not contribute to the gut immune system in man | Q74704872 | ||
Intestinal IgA plasma cells of the B1 lineage are IL-5 dependent | Q77312741 | ||
Loss of ileal IgA+ plasma cells and of CD4+ lymphocytes in ileal Peyer's patches of vitamin A deficient rats | Q78576579 | ||
Structural and functional differences between putative mucosal inductive sites of the rat | Q78852110 | ||
CD11b+ Peyer’s Patch Dendritic Cells Secrete IL-6 and Induce IgA Secretion from Naive B Cells | Q79074376 | ||
Enhanced IgA class switching in marginal zone and B1 B cells relative to follicular/B2 B cells | Q79287428 | ||
TACI regulates IgA production by APRIL in collaboration with HSPG | Q79374551 | ||
Intestinal IgA synthesis: a primitive form of adaptive immunity that regulates microbial communities in the gut | Q79426180 | ||
Extrafollicular activation of lymph node B cells by antigen-bearing dendritic cells | Q79734101 | ||
The peritoneal micromilieu commits B cells to home to body cavities and the small intestine | Q79749943 | ||
TGF-beta receptor signaling is critical for mucosal IgA responses | Q80475685 | ||
CC chemokine ligands 25 and 28 play essential roles in intestinal extravasation of IgA antibody-secreting cells | Q80542422 | ||
B cells acquire particulate antigen in a macrophage-rich area at the boundary between the follicle and the subcapsular sinus of the lymph node | Q80688189 | ||
Lamina propria macrophages and dendritic cells differentially induce regulatory and interleukin 17-producing T cell responses | Q81305086 | ||
Dendritic cells govern induction and reprogramming of polarized tissue-selective homing receptor patterns of T cells: important roles for soluble factors and tissue microenvironments | Q81456293 | ||
Cell surface recycling of internalized antigen permits dendritic cell priming of B cells | Q81476297 | ||
Subcapsular encounter and complement-dependent transport of immune complexes by lymph node B cells. | Q46017170 | ||
Interleukin 5 is a differentiation factor for IgA B cells | Q46343883 | ||
L-selectin-mediated lymphocyte rolling on MAdCAM-1. | Q46407093 | ||
alpha 4 integrins mediate lymphocyte attachment and rolling under physiologic flow | Q46523925 | ||
Distinct roles of L-selectin and integrins alpha 4 beta 7 and LFA-1 in lymphocyte homing to Peyer's patch-HEV in situ: the multistep model confirmed and refined | Q46550913 | ||
Role of gut-associated lymphoreticular tissues in antigen-specific intestinal IgA immunity | Q47232033 | ||
IgA class switch occurs in the organized nasopharynx- and gut-associated lymphoid tissue, but not in the diffuse lamina propria of airways and gut. | Q47644148 | ||
Plasmacytoid dendritic cells, antigen, and CpG-C license human B cells for plasma cell differentiation and immunoglobulin production in the absence of T-cell help | Q47800822 | ||
B1 Cells Contribute to Serum IgM, But Not to Intestinal IgA, Production in Gnotobiotic Ig Allotype Chimeric Mice | Q47960223 | ||
Induction of protective IgA by intestinal dendritic cells carrying commensal bacteria | Q47962035 | ||
Isolated lymphoid follicles are not IgA inductive sites for recombinant Salmonella | Q50070717 | ||
Unique characteristics of the intestinal immune system as an inductive site after antigen reencounter. | Q50094459 | ||
Vaccine-induced protection against gastrointestinal bacterial infections in the absence of secretory antibodies | Q50094621 | ||
IgA production without mu or delta chain expression in developing B cells | Q50114613 | ||
Retinoic acid and host-pathogen interactions: effects on inducible nitric oxide synthase in vivo | Q50118666 | ||
Homing potentials of circulating antibody-secreting cells after administration of oral or parenteral protein or polysaccharide vaccine in humans | Q50127622 | ||
VH1-46 is the dominant immunoglobulin heavy chain gene segment in rotavirus-specific memory B cells expressing the intestinal homing receptor alpha4beta7. | Q51993784 | ||
Activated primary and memory CD8 T cells migrate to nonlymphoid tissues regardless of site of activation or tissue of origin. | Q52001463 | ||
Maintenance of serological memory by polyclonal activation of human memory B cells. | Q52008907 | ||
Intestinal dendritic cells increase T cell expression of alpha4beta7 integrin. | Q52013140 | ||
Correlation of tissue distribution, developmental phenotype, and intestinal homing receptor expression of antigen-specific B cells during the murine anti-rotavirus immune response. | Q52014286 | ||
IgA production by peritoneal cavity B cells is IL-6 independent: implications for intestinal IgA responses. | Q52508737 | ||
Impaired immune and acute-phase responses in interleukin-6-deficient mice. | Q52514391 | ||
Is long-term humoral immunity in the mucosa provided by long-lived plasma cells? A question still open. | Q52933267 | ||
Regulation of IgA production by naturally occurring TNF/iNOS-producing dendritic cells. | Q53026421 | ||
Gut IgA class switch recombination in the absence of CD40 does not occur in the lamina propria and is independent of germinal centers. | Q54570939 | ||
Human intestinal IgA response is generated in the organized gut-associated lymphoid tissue but not in the lamina propria. | Q54660349 | ||
Secretory antibodies reduce systemic antibody responses against the gastrointestinal commensal flora | Q57135946 | ||
Critical role for β7 integrins in formation of the gut-associated lymphoid tissue | Q57198355 | ||
An Essential Role for BAFF in the Normal Development of B Cells Through a BCMA-Independent Pathway | Q57230082 | ||
Intestinal Bacteria Trigger T Cell-Independent Immunoglobulin A2 Class Switching by Inducing Epithelial-Cell Secretion of the Cytokine APRIL | Q58493951 | ||
Human rotavirus specific T cells: quantification by ELISPOT and expression of homing receptors on CD4+ T cells | Q60321337 | ||
Different pathways of differentiation of pre-B cell lines are induced by dendritic cells and T cells from different lymphoid tissues. | Q64990342 | ||
Role of IL-6 in Human Antigen-Specific and Polyclonal IgA Responses | Q67882926 | ||
Many of the IgA producing plasma cells in murine gut are derived from self-replenishing precursors in the peritoneal cavity | Q69152049 | ||
A major peritoneal reservoir of precursors for intestinal IgA plasma cells | Q69739699 | ||
Localization of transforming growth factor beta isoforms in the normal murine small intestine and colon | Q70767763 | ||
Novel synthetic retinoic acid inhibits rat collagen arthritis and differentially affects serum immunoglobulin subclass levels | Q70869160 | ||
Human intestinal B-cell blasts and plasma cells express the mucosal homing receptor integrin alpha 4 beta 7 | Q70877525 | ||
Expression of transforming growth factors alpha and beta in colonic mucosa in inflammatory bowel disease | Q71035783 | ||
Endogenous cytokine expression profiles in retinoic acid-induced IgA production by LPS-stimulated murine splenocytes | Q71581571 | ||
Vasoactive intestinal peptide specifically induces human IgA1 and IgA2 production | Q71646944 | ||
Increased mortality in children with mild vitamin A deficiency | Q72560411 | ||
Retinoids enhance IgA production by lipopolysaccharide-stimulated murine spleen cells | Q72920569 | ||
TGF-beta receptor controls B cell responsiveness and induction of IgA in vivo | Q73168724 | ||
Vitamin A deficiency leads to severe functional disturbance of the intestinal epithelium enzymes associated with diarrhoea and increased bacterial translocation in gnotobiotic rats | Q73371098 | ||
Neuronal nitric oxide synthase activation by vasoactive intestinal peptide in bovine cerebral arteries | Q73723850 | ||
Cutting edge: the B cell chemokine CXC chemokine ligand 13/B lymphocyte chemoattractant is expressed in the high endothelial venules of lymph nodes and Peyer's patches and affects B cell trafficking across high endothelial venules | Q73765073 | ||
A hallmark of active class switch recombination: transcripts directed by I promoters on looped-out circular DNAs | Q33947941 | ||
Generation of gut-homing IgA-secreting B cells by intestinal dendritic cells | Q34000967 | ||
The functional interactions of commensal bacteria with intestinal secretory IgA. | Q34007246 | ||
Expression of cutaneous lymphocyte-associated antigen and E-selectin ligand by circulating human memory CD4+ T lymphocytes specific for herpes simplex virus type 2. | Q34081662 | ||
Homing in on the cellular immune response to HSV-2 in humans. | Q34081670 | ||
Oral immunization with a Salmonella enterica serovar typhi vaccine induces specific circulating mucosa-homing CD4(+) and CD8(+) T cells in humans | Q34131647 | ||
Selective imprinting of gut-homing T cells by Peyer's patch dendritic cells | Q34211233 | ||
Dysregulated interleukin 6 expression produces a syndrome resembling Castleman's disease in mice. | Q34259037 | ||
A cell-surface molecule involved in organ-specific homing of lymphocytes | Q34272163 | ||
Retinoic acid: an educational "vitamin elixir" for gut-seeking T cells | Q34358924 | ||
Vitamin A deficiency increases inflammatory responses | Q34411507 | ||
The B-cell system in inflammatory bowel disease | Q34514530 | ||
Expression of cutaneous lymphocyte-associated antigen by CD8(+) T cells specific for a skin-tropic virus | Q34777218 | ||
Homing of antibody secreting cells | Q35170914 | ||
Plasma-cell homing | Q35549150 | ||
Antigen-specific memory B cell development | Q36072438 | ||
Immunohistologic and functional characterization of a vascular addressin involved in lymphocyte homing into peripheral lymph nodes | Q36219735 | ||
Innate secretory antibodies protect against natural Salmonella typhimurium infection | Q36227913 | ||
Regulation of AID expression in the immune response | Q36229307 | ||
The life span of IgA plasma cells from the mouse intestine | Q36272489 | ||
The origin and antigen-dependent distribution of IgA-containing cells in the intestine | Q36342073 | ||
Preferential induction of polyclonal IgA secretion by murine Peyer's patch dendritic cell-T cell mixtures | Q36349156 | ||
Interleukins and IgA synthesis. Human and murine interleukin 6 induce high rate IgA secretion in IgA-committed B cells | Q36356413 | ||
Transforming growth factor beta specifically enhances IgA production by lipopolysaccharide-stimulated murine B lymphocytes | Q36356779 | ||
Lymphocyte migration in lymphocyte function-associated antigen (LFA)-1-deficient mice | Q36368167 | ||
Identification of CD22 ligands on bone marrow sinusoidal endothelium implicated in CD22-dependent homing of recirculating B cells | Q36368171 | ||
A coordinated change in chemokine responsiveness guides plasma cell movements | Q36369352 | ||
Migratory properties of naive, effector, and memory CD8(+) T cells | Q36369485 | ||
The intestinal chemokine thymus-expressed chemokine (CCL25) attracts IgA antibody-secreting cells | Q36369860 | ||
Chemokine requirements for B cell entry to lymph nodes and Peyer's patches. | Q36371105 | ||
Freshly isolated Peyer's patch, but not spleen, dendritic cells produce interleukin 10 and induce the differentiation of T helper type 2 cells | Q36375116 | ||
The role of chemokines in the microenvironmental control of T versus B cell arrest in Peyer's patch high endothelial venules | Q36375848 | ||
The CC chemokine thymus-derived chemotactic agent 4 (TCA-4, secondary lymphoid tissue chemokine, 6Ckine, exodus-2) triggers lymphocyte function-associated antigen 1-mediated arrest of rolling T lymphocytes in peripheral lymph node high endothelial v | Q36375878 | ||
Chemokine receptor CCR9 contributes to the localization of plasma cells to the small intestine | Q36399163 | ||
Molecular mechanisms of lymphocyte homing to peripheral lymph nodes | Q36400133 | ||
TACI and BAFF-R mediate isotype switching in B cells | Q36402479 | ||
Reciprocal and dynamic control of CD8 T cell homing by dendritic cells from skin- and gut-associated lymphoid tissues | Q36402630 | ||
Impact of vitamin A supplementation on childhood mortality. A randomised controlled community trial | Q36414513 | ||
Roundtrip ticket for secretory IgA: role in mucosal homeostasis? | Q36689578 | ||
Gut lymphocyte migration: we are halfway 'home'. | Q36733381 | ||
The clinical significance of immunoglobulin A deficiency | Q36760481 | ||
Loss of integrin alpha(v)beta8 on dendritic cells causes autoimmunity and colitis in mice | Q37161107 | ||
Vasoactive intestinal peptide induces S(alpha)/S(mu) switch circular DNA in human B cells | Q37360187 | ||
Differential expression of tissue-specific adhesion molecules on human circulating antibody-forming cells after systemic, enteric, and nasal immunizations. A molecular basis for the compartmentalization of effector B cell responses | Q37365152 | ||
Expression of mucosal homing receptor alpha4beta7 by circulating CD4+ cells with memory for intestinal rotavirus | Q37371917 | ||
Role of interleukin-6 in human and mouse mucosal IgA plasma cell responses | Q37532241 | ||
Retinoic acid activates human inducible nitric oxide synthase gene through binding of RARalpha/RXRalpha heterodimer to a novel retinoic acid response element in the promoter | Q38304594 | ||
The liver and IgA: immunological, cell biological and clinical implications | Q38619047 | ||
Effect of periodic vitamin A supplementation on mortality and morbidity of human immunodeficiency virus-infected children in Uganda: A controlled clinical trial | Q38881348 | ||
CCL25 mediates the localization of recently activated CD8alphabeta(+) lymphocytes to the small-intestinal mucosa | Q39737286 | ||
Subcapsular sinus macrophages in lymph nodes clear lymph-borne viruses and present them to antiviral B cells | Q40068378 | ||
Beta-carotene storage, conversion to retinoic acid, and induction of the lipocyte phenotype in hepatic stellate cells | Q40562969 | ||
Rotavirus-specific B cells induced by recent infection in adults and children predominantly express the intestinal homing receptor alpha4beta7. | Q40613333 | ||
Alpha 4 beta 7 integrin mediates lymphocyte binding to the mucosal vascular addressin MAdCAM-1. | Q41541656 | ||
Rapid active transport of immunoglobulin A from blood to bile | Q41962947 | ||
Regulation of B1 cell migration by signals through Toll-like receptors | Q41974270 | ||
Transforming growth factor beta induces IgA production and acts additively with interleukin 5 for IgA production | Q42062033 | ||
Defective B-1 cell development and impaired immunity against Angiostrongylus cantonensis in IL-5R alpha-deficient mice | Q42517634 | ||
Transforming growth factor-beta 1 (TGF-beta 1) is a bifunctional immune regulator for mucosal IgA responses | Q43562701 | ||
The mucosal vascular addressin is a tissue-specific endothelial cell adhesion molecule for circulating lymphocytes | Q43606018 | ||
Impaired vitamin A-mediated mucosal IgA response in IL-5 receptor-knockout mice. | Q43667875 | ||
In situ class switching and differentiation to IgA-producing cells in the gut lamina propria | Q43776134 | ||
Priming of CTLs by lymphocytic choriomeningitis virus depends on dendritic cells | Q43845179 | ||
IgG plasma cells display a unique spectrum of leukocyte adhesion and homing molecules | Q43945188 | ||
Enhancement of the inducible NO synthase activation by retinoic acid is mimicked by RARalpha agonist in vivo | Q44095712 | ||
Dynamic programming of CD8+ T cell trafficking after live viral immunization | Q44181883 | ||
B cell-specific deficiency for Smad2 in vivo leads to defects in TGF-beta-directed IgA switching and changes in B cell fate | Q44248689 | ||
Macrophage- and dendritic cell--dependent regulation of human B-cell proliferation requires the TNF family ligand BAFF. | Q44280905 | ||
In vitro induction of mucosa-type dendritic cells by all-trans retinoic acid | Q44404322 | ||
Lung retinol storing cells synthesize and secrete retinoic acid, an inducer of alveolus formation | Q44495192 | ||
Dendritic cell immunization route determines CD8+ T cell trafficking to inflamed skin: role for tissue microenvironment and dendritic cells in establishment of T cell-homing subsets | Q44714977 | ||
Inflammation location, but not type, determines the increase in TGF-beta1 and IGF-1 expression and collagen deposition in IBD intestine | Q44924237 | ||
Vitamin A deficiency has different effects on immunoglobulin A production and transport during influenza A infection in BALB/c mice | Q45238829 | ||
Cutaneous lymphocyte antigen expression on human effector B cells depends on the site and on the nature of antigen encounter | Q45256434 | ||
Vitamin A deficiency diminishes the salivary immunoglobulin A response and enhances the serum immunoglobulin G response to influenza A virus infection in BALB/c mice | Q45772126 | ||
The role of interleukin-6 in mucosal IgA antibody responses in vivo | Q45872747 | ||
P433 | issue | 2 | |
P304 | page(s) | 96-109 | |
P577 | publication date | 2008-01-23 | |
P1433 | published in | Mucosal Immunology | Q15817743 |
P1476 | title | Differentiation and homing of IgA-secreting cells | |
P478 | volume | 1 |
Q61444207 | A Novel Supplementation Approach to Enhance Host Response to Sublingual Vaccination |
Q54238056 | A guide to chemokines and their receptors. |
Q36769690 | ATG5 regulates plasma cell differentiation |
Q38126789 | Advances in the treatment of coeliac disease: an immunopathogenic perspective |
Q34490479 | B cell homeostasis and plasma cell homing controlled by Krüppel-like factor 2. |
Q41813088 | Blocking lymphocyte localization to the gastrointestinal mucosa as a therapeutic strategy for inflammatory bowel diseases |
Q38017619 | CCR10 and its ligands in regulation of epithelial immunity and diseases |
Q49965403 | CD103+CD11b+ mucosal classical dendritic cells initiate long-term switched antibody responses to flagellin |
Q89481420 | CX3CR1+ Macrophages and CD8+ T Cells Control Intestinal IgA Production |
Q33693196 | CXCR4/IgG-expressing plasma cells are associated with human gastrointestinal tissue inflammation |
Q38574884 | Cellular and chromatin dynamics of antibody-secreting plasma cells |
Q92603366 | Changes in the small intestine mucosal immune barrier in Muscovy ducklings infected with Muscovy duck reovirus |
Q33596284 | Chloroplast-derived vaccine antigens confer dual immunity against cholera and malaria by oral or injectable delivery |
Q35091189 | Clonally related CD8+ T cells responsible for rapid population of both diffuse nasal-associated lymphoid tissue and lung after respiratory virus infection |
Q39921289 | Cocoa and cocoa fibre differentially modulate IgA and IgM production at mucosal sites. |
Q54379579 | Cocoa-enriched diets modulate intestinal and systemic humoral immune response in young adult rats. |
Q53706620 | Commensal Microbes Induce Serum IgA Responses that Protect against Polymicrobial Sepsis. |
Q40205180 | Comparison of interferon and bovine herpesvirus-1-specific IgA levels in nasal secretions of dairy cattle administered an intranasal modified live viral vaccine prior to calving or on the day of calving. |
Q38675016 | Compartmentalization of immunosenescence: a deeper look at the mucosa |
Q33893588 | Control of lupus nephritis by changes of gut microbiota. |
Q98287666 | Coordinated co-migration of CCR10+ antibody-producing B cells with helper T cells for colonic homeostatic regulation |
Q40278762 | Cross-reactive gut-directed immune response against Salmonella enterica serovar Paratyphi A and B in typhoid fever and after oral Ty21a typhoid vaccination |
Q40222613 | Cross-reactive immune response induced by the Vi capsular polysaccharide typhoid vaccine against Salmonella Paratyphi strains |
Q99633171 | Cytokine storm in aged people with CoV-2: possible role of vitamins as therapy or preventive strategy |
Q60956974 | Defensive Driving: Directing HIV-1 Vaccine-Induced Humoral Immunity to the Mucosa with Chemokine Adjuvants |
Q39278063 | Dendritic cell-targeting DNA-based nasal adjuvants for protective mucosal immunity to Streptococcus pneumoniae |
Q30396642 | Development of adenoviral vector-based mucosal vaccine against influenza |
Q89748559 | Distinct microbial and immune niches of the human colon |
Q35754076 | Distribution of immunoglobulin G antibody secretory cells in small intestine of Bactrian camels (Camelus bactrianus) |
Q38965462 | Effect of a cocoa diet on the small intestine and gut-associated lymphoid tissue composition in an oral sensitization model in rats |
Q37950457 | Endogenous migration modulators as parent compounds for the development of novel cardiovascular and anti-inflammatory drugs |
Q37770212 | Enemy at the gates: dendritic cells and immunity to mucosal pathogens |
Q35952010 | Epithelial expression of the cytosolic retinoid chaperone cellular retinol binding protein II is essential for in vivo imprinting of local gut dendritic cells by lumenal retinoids |
Q36850687 | Food components and the immune system: from tonic agents to allergens |
Q91986433 | Formulation technologies for oral vaccines |
Q37744898 | Function of mucosa-associated lymphoid tissue in antibody formation |
Q35144035 | Generation of colonic IgA-secreting cells in the caecal patch. |
Q34068059 | Gut-Homing Conventional Plasmablasts and CD27(-) Plasmablasts Elicited after a Short Time of Exposure to an Oral Live-Attenuated Shigella Vaccine Candidate in Humans |
Q101226750 | Gut-educated IgA plasma cells defend the meningeal venous sinuses |
Q39349334 | Immunological Functions of the Omentum |
Q34567202 | Immunomodulatory activity of Bengkoang (Pachyrhizus erosus) fiber extract in vitro and in vivo |
Q35366334 | Impact of cocoa polyphenol extracts on the immune system and microbiota in two strains of young rats. |
Q35618515 | Impaired Antibody-mediated Protection and Defective IgA B-Cell Memory in Experimental Infection of Adults with Respiratory Syncytial Virus |
Q41050295 | Improved immune responses to a bivalent vaccine of Newcastle disease and avian influenza in chickens by ginseng stem-leaf saponins |
Q45373993 | Increases in IgA+ B cells in Peyer's patches during milk-borne mouse mammary tumor virus infection are influenced by Toll-like receptor 4 and are completely dependent on the superantigen response |
Q39384289 | Inducing Mucosal IgA: A Challenge for Vaccine Adjuvants and Delivery Systems |
Q89574814 | Induction of systemic immunity through nasal-associated lymphoid tissue (NALT) of mice intranasally immunized with Brucella abortus malate dehydrogenase-loaded chitosan nanoparticles |
Q34614189 | Innate signaling networks in mucosal IgA class switching |
Q39652835 | Intake of black-vinegar-mash-garlic enhances salivary release of secretory IgA: A randomized, double-blind, placebo-controlled, parallel-group study |
Q38190874 | Intestinal epithelial cells: regulators of barrier function and immune homeostasis |
Q50907644 | LRRK2: An Emerging New Molecule in the Enteric Neuronal System That Quantitatively Regulates Neuronal Peptides and IgA in the Gut. |
Q36592984 | Leukocyte Trafficking to the Small Intestine and Colon |
Q40270837 | Live oral typhoid vaccine Salmonella Typhi Ty21a - a surrogate vaccine against non-typhoid salmonella? |
Q36506867 | Lymphotoxin alpha-deficient mice clear persistent rotavirus infection after local generation of mucosal IgA |
Q57126727 | Mesenteric lymph nodes are not required for an intestinal immunoglobulin A response to oral cholera toxin |
Q88752692 | More robust gut immune responses induced by combining intranasal and sublingual routes for prime-boost immunization |
Q38271434 | Mucosal Immunity and acute viral gastroenteritis |
Q33681946 | Mucosal T-cell responses to HIV: responding at the front lines |
Q34797176 | Mucosal application of gp140 encoding DNA polyplexes to different tissues results in altered immunological outcomes in mice. |
Q38028996 | Mucosal immunity and nasal influenza vaccination |
Q37137068 | Mucosal immunity to HIV: a review of recent literature |
Q34713905 | Mucosal immunology of food allergy |
Q44938493 | Natalizumab treatment decreases serum IgM and IgG levels in multiple sclerosis patients |
Q37505746 | Oral administration of Lactobacillus plantarum strain AYA enhances IgA secretion and provides survival protection against influenza virus infection in mice |
Q33412526 | Oral administration of Shiga toxin-producing Escherichia coli induces intestinal and systemic specific immune response in mice |
Q37634776 | Oral administration of heat-killed Lactobacillus kunkeei YB38 improves murine influenza pneumonia by enhancing IgA production. |
Q63729523 | Parenteral Vaccination With a Tuberculosis Subunit Vaccine in Presence of Retinoic Acid Provides Early but Transient Protection to M. Tuberculosis Infection |
Q57030977 | Participation of the spleen in the IgA immune response in the gut |
Q35726077 | Persistence of diarrheal pathogens is associated with continued recruitment of plasmablasts in the circulation |
Q36810325 | Peyer's patches: organizing B-cell responses at the intestinal frontier |
Q37615056 | Phenotypes and functions of persistent Sendai virus-induced antibody forming cells and CD8+ T cells in diffuse nasal-associated lymphoid tissue typify lymphocyte responses of the gut |
Q38722252 | Plasmablasts with a mucosal phenotype contribute to plasmacytosis in SLE. |
Q34168838 | Plasmodium falciparum malaria and invasive bacterial co-infection in young African children: the dysfunctional spleen hypothesis. |
Q61807004 | Profiling the Atlantic Salmon IgM B Cell Surface Proteome: Novel Information on Teleost Fish B Cell Protein Repertoire and Identification of Potential B Cell Markers |
Q41027192 | Psychological distress and salivary secretory immunity. |
Q34347803 | Putting J chain back on the map: how might its expression define plasma cell development? |
Q33575069 | Randomized, double-blind, placebo-controlled, parallel-group study of the effect of Lactobacillus paracasei K71 intake on salivary release of secretory immunoglobulin A. |
Q38029250 | Recent progress in mucosal vaccine development: potential and limitations |
Q58202682 | Rediscovering IgA |
Q35940739 | Reduced frequencies and heightened CD103 expression among virus-induced CD8(+) T cells in the respiratory tract airways of vitamin A-deficient mice |
Q35778680 | Regulation of intestinal IgA responses |
Q35880427 | Retinoic Acid Differentially Regulates the Migration of Innate Lymphoid Cell Subsets to the Gut. |
Q37564860 | Rhesus macaque rectal and duodenal tissues exhibit B-cell sub-populations distinct from peripheral blood that continuously secrete antigen-specific IgA in short-term explant cultures |
Q34175747 | Robust IgA and IgG-producing antibody forming cells in the diffuse-NALT and lungs of Sendai virus-vaccinated cotton rats associate with rapid protection against human parainfluenza virus-type 1 |
Q37274255 | Role of retinoic acid in the imprinting of gut-homing IgA-secreting cells |
Q48140617 | S1P Signalling Differentially Affects Migration of Peritoneal B Cell Populations In Vitro and Influences the Production of Intestinal IgA In Vivo. |
Q64376875 | Safety and immunogenicity of an oral tablet norovirus vaccine, a phase I randomized, placebo-controlled trial |
Q88875501 | Secondary IgA nephropathy |
Q40181057 | Specific and cross-reactive immune response to oral Salmonella Typhi Ty21a and parenteral Vi capsular polysaccharide typhoid vaccines administered concomitantly |
Q37435066 | Systemic and mucosal immune responses following oral adenoviral delivery of influenza vaccine to the human intestine by radio controlled capsule |
Q37744904 | T cell-dependent and -independent IgA responses: role of TLR signalling |
Q54476546 | TBK1 suppression of IgA in the NIK of time. |
Q92815883 | The Pleiotropic Role of Retinoic Acid/Retinoic Acid Receptors Signaling: From Vitamin A Metabolism to Gene Rearrangements in Acute Promyelocytic Leukemia |
Q41184465 | The Role of Integrin Expressing Cells in Modulating Disease Susceptibility and Progression (January 2016). |
Q41457100 | The effects of cocoa on the immune system |
Q38989513 | The long and winding road to IgA deficiency: causes and consequences. |
Q36152172 | The suckling rat as a model for immunonutrition studies in early life |
Q26825413 | Therapeutic approaches for celiac disease |
Q34610624 | Vaccination strategies to promote mucosal antibody responses. |
Q36144543 | Vitamin A deficiency disrupts vaccine-induced antibody-forming cells and the balance of IgA/IgG isotypes in the upper and lower respiratory tract |
Q40935197 | Vitamin A deficient mice exhibit increased viral antigens and enhanced cytokine/chemokine production in nasal tissues following respiratory virus infection despite the presence of FoxP3+ T cells |
Q34005584 | Vitamin effects on the immune system: vitamins A and D take centre stage |
Q38113207 | What is and what should always have been: long-lived plasma cells induced by T cell-independent antigens |
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