| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Reza Motallebzadeh | Q58305723 |
| Gavin J Pettigrew | Q60057250 | ||
| P2093 | author name string | Jawaher Alsughayyir | |
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| Generation of T follicular helper cells is mediated by interleukin-21 but independent of T helper 1, 2, or 17 cell lineages | Q24642180 | ||
| B cell attracting chemokine 1 (CXCL13) and its receptor CXCR5 are expressed in normal and aberrant gut associated lymphoid tissue | Q24669900 | ||
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| IL-17 and Th17 Cells | Q27860566 | ||
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| BCA-1/CXCL13 expression is associated with CXCR5-positive B-cell cluster formation in acute renal transplant rejection | Q28240808 | ||
| Characterization of surface lymphotoxin forms. Use of specific monoclonal antibodies and soluble receptors | Q28242865 | ||
| EBI2 mediates B cell segregation between the outer and centre follicle | Q28251850 | ||
| Bcl6 and Blimp-1 are reciprocal and antagonistic regulators of T follicular helper cell differentiation | Q28252247 | ||
| High endothelial venules (HEVs): specialized endothelium for lymphocyte migration | Q28288508 | ||
| A RING-type ubiquitin ligase family member required to repress follicular helper T cells and autoimmunity | Q28507088 | ||
| Overlapping roles of CXCL13, interleukin 7 receptor alpha, and CCR7 ligands in lymph node development | Q28585776 | ||
| SAP is required for generating long-term humoral immunity | Q28588045 | ||
| Lymph node fibroblastic reticular cells construct the stromal reticulum via contact with lymphocytes | Q28590628 | ||
| EBI2 augments Tfh cell fate by promoting interaction with IL-2-quenching dendritic cells | Q28591068 | ||
| Chemokines and their receptors in human renal allotransplantation | Q35848818 | ||
| Tertiary Lymphoid Tissue Forms in Retinas of Mice with Spontaneous Autoimmune Uveitis and Has Consequences on Visual Function | Q35880301 | ||
| IL-22 regulates lymphoid chemokine production and assembly of tertiary lymphoid organs | Q36055624 | ||
| A stromal address code defined by fibroblasts | Q36061032 | ||
| The receptor Ly108 functions as a SAP adaptor-dependent on-off switch for T cell help to B cells and NKT cell development | Q36074906 | ||
| IL-17-dependent cellular immunity to collagen type V predisposes to obliterative bronchiolitis in human lung transplants | Q36088927 | ||
| B cell proliferation, somatic hypermutation, class switch recombination, and autoantibody production in ectopic lymphoid tissue in murine lupus | Q36091161 | ||
| CCL21 expression pattern of human secondary lymphoid organ stroma is conserved in inflammatory lesions with lymphoid neogenesis. | Q36095617 | ||
| Th17 cells induce ectopic lymphoid follicles in central nervous system tissue inflammation | Q36174679 | ||
| Interleukin-27 inhibits ectopic lymphoid-like structure development in early inflammatory arthritis. | Q36180696 | ||
| Two sides of a cellular coin: CD4(+)CD3- cells regulate memory responses and lymph-node organization | Q36202186 | ||
| Immunohistologic and functional characterization of a vascular addressin involved in lymphocyte homing into peripheral lymph nodes | Q36219735 | ||
| High affinity germinal center B cells are actively selected into the plasma cell compartment. | Q36228042 | ||
| Antigen recognition strength regulates the choice between extrafollicular plasma cell and germinal center B cell differentiation | Q36228608 | ||
| Follicular dendritic cells in health and disease | Q36250237 | ||
| Inducible tertiary lymphoid structures, autoimmunity, and exocrine dysfunction in a novel model of salivary gland inflammation in C57BL/6 mice | Q36253046 | ||
| The T cell-B cell interaction via OX40-OX40L is necessary for the T cell-dependent humoral immune response | Q36365985 | ||
| Chronic inflammation caused by lymphotoxin is lymphoid neogenesis | Q36366337 | ||
| Regulation of peripheral lymph node genesis by the tumor necrosis factor family member TRANCE | Q36368551 | ||
| Intrinsic constraint on plasmablast growth and extrinsic limits of plasma cell survival | Q36368882 | ||
| CD8 T cells are required for the formation of ectopic germinal centers in rheumatoid synovitis | Q36370272 | ||
| Ectopic LTαβ Directs Lymphoid Organ Neogenesis with Concomitant Expression of Peripheral Node Addressin and a HEV-restricted Sulfotransferase | Q36370988 | ||
| The sequential role of lymphotoxin and B cells in the development of splenic follicles. | Q36400592 | ||
| Lymphoid neogenesis in chronic inflammatory diseases. | Q36405080 | ||
| Analysis of a wild mouse promoter variant reveals a novel role for FcγRIIb in the control of the germinal center and autoimmunity. | Q36409027 | ||
| A Temporal Switch in the Germinal Center Determines Differential Output of Memory B and Plasma Cells | Q36494525 | ||
| Follicular regulatory T cells can be specific for the immunizing antigen and derive from naive T cells. | Q36536511 | ||
| Local T/B cooperation in inflamed tissues is supported by T follicular helper-like cells. | Q36637198 | ||
| EAF2 mediates germinal centre B-cell apoptosis to suppress excessive immune responses and prevent autoimmunity. | Q36661580 | ||
| Complex Antigens Drive Permissive Clonal Selection in Germinal Centers | Q36693170 | ||
| Independent Roles of Switching and Hypermutation in the Development and Persistence of B Lymphocyte Memory | Q36818340 | ||
| Circulating fibrocytes traffic to the lungs in response to CXCL12 and mediate fibrosis | Q36849123 | ||
| Augmentation of Recipient Adaptive Alloimmunity by Donor Passenger Lymphocytes within the Transplant | Q36910447 | ||
| Ubiquitin-mediated fluctuations in MHC class II facilitate efficient germinal center B cell responses | Q36949908 | ||
| CD4⁺ follicular helper T cell infiltration predicts breast cancer survival | Q36966923 | ||
| CD4 T cell epitope specificity determines follicular versus non-follicular helper differentiation in the polyclonal response to influenza infection or vaccination | Q37027382 | ||
| The highway code of T cell trafficking. | Q37045760 | ||
| Ectopic lymphoid tissues and local immunity | Q37075235 | ||
| Visualizing antibody affinity maturation in germinal centers | Q37078589 | ||
| Lymphoid tissue formation in allografts: innocent until proven guilty. | Q37095193 | ||
| SAP-controlled T-B cell interactions underlie germinal centre formation | Q37119530 | ||
| The role of IL-21 in regulating B-cell function in health and disease. | Q37211251 | ||
| Follicular helper T cells are required for systemic autoimmunity | Q37234304 | ||
| The function of follicular helper T cells is regulated by the strength of T cell antigen receptor binding | Q37266009 | ||
| Visualizing B cell capture of cognate antigen from follicular dendritic cells | Q37273220 | ||
| Single cell cloning and recombinant monoclonal antibodies generation from RA synovial B cells reveal frequent targeting of citrullinated histones of NETs. | Q37282551 | ||
| Germinal center centroblasts transition to a centrocyte phenotype according to a timed program and depend on the dark zone for effective selection. | Q37309590 | ||
| Invariant natural killer T cells direct B cell responses to cognate lipid antigen in an IL-21-dependent manner | Q37322505 | ||
| Antigen-driven clonal proliferation of B cells within the target tissue of an autoimmune disease. The salivary glands of patients with Sjögren's syndrome | Q37384819 | ||
| Colocalization of antigen-specific B and T cells within ectopic lymphoid tissue following immunization with exogenous antigen | Q37403161 | ||
| Involvement of lymphoid inducer cells in the development of secondary and tertiary lymphoid structure | Q37464319 | ||
| Local BLyS production by T follicular cells mediates retention of high affinity B cells during affinity maturation | Q37483106 | ||
| New insights into the differentiation and function of T follicular helper cells. | Q37621244 | ||
| Dysregulation of germinal centres in autoimmune disease. | Q37638196 | ||
| Different B cell populations mediate early and late memory during an endogenous immune response | Q37712769 | ||
| FcgammaRIIB in autoimmunity and infection: evolutionary and therapeutic implications. | Q37736263 | ||
| New insights into the development of lymphoid tissues | Q37779724 | ||
| B-cell stage and context-dependent requirements for survival signals from BAFF and the B-cell receptor. | Q37781397 | ||
| Impaired clearance of apoptotic cells in germinal centers: implications for loss of B cell tolerance and induction of autoimmunity | Q37950925 | ||
| Tertiary lymphoid organs in infection and autoimmunity | Q38012568 | ||
| BAFF and associated TNF superfamily members in renal transplantation: an end to BLySful ignorance | Q38115122 | ||
| Follicular dendritic cells: origin, phenotype, and function in health and disease | Q38169426 | ||
| Ectopic lymphoid-like structures in infection, cancer and autoimmunity | Q38221815 | ||
| Tertiary lymphoid structures in cancer and beyond | Q38274486 | ||
| Stromal cells in chronic inflammation and tertiary lymphoid organ formation | Q38415281 | ||
| Characterization of intra-graft B cells during renal allograft rejection | Q38426194 | ||
| The conduit system transports soluble antigens from the afferent lymph to resident dendritic cells in the T cell area of the lymph node | Q38459394 | ||
| The transcription factor BATF controls the global regulators of class-switch recombination in both B cells and T cells | Q28593666 | ||
| IL-23 drives a pathogenic T cell population that induces autoimmune inflammation | Q29547525 | ||
| Fcgamma receptors as regulators of immune responses | Q29615584 | ||
| CTLA-4 control over Foxp3+ regulatory T cell function | Q29619413 | ||
| Lymphocyte homing and homeostasis | Q29619924 | ||
| Stromal cell networks regulate lymphocyte entry, migration, and territoriality in lymph nodes | Q29620381 | ||
| Lymphatic neoangiogenesis in human kidney transplants is associated with immunologically active lymphocytic infiltrates | Q30090232 | ||
| Development and migration of plasma cells in the mouse lymph node | Q30496934 | ||
| Germinal center dynamics revealed by multiphoton microscopy with a photoactivatable fluorescent reporter | Q30498133 | ||
| The sphingosine 1-phosphate receptor S1P₂ maintains the homeostasis of germinal center B cells and promotes niche confinement | Q30503547 | ||
| T follicular helper cell dynamics in germinal centers | Q30573316 | ||
| Sphingosine-1-phosphate receptor 2 is critical for follicular helper T cell retention in germinal centers. | Q30582101 | ||
| In vivo imaging of germinal centres reveals a dynamic open structure | Q33271310 | ||
| Lymphotoxin beta receptor signaling promotes tertiary lymphoid organogenesis in the aorta adventitia of aged ApoE-/- mice | Q33399367 | ||
| Germinal center reutilization by newly activated B cells | Q33590462 | ||
| Differentiation of B cells in the nonlymphoid tissue of the synovial membrane of patients with rheumatoid arthritis | Q33611035 | ||
| IL-21 regulates germinal center B cell differentiation and proliferation through a B cell-intrinsic mechanism | Q33656121 | ||
| IL-21 acts directly on B cells to regulate Bcl-6 expression and germinal center responses | Q33656146 | ||
| Optimal germinal center responses require a multistage T cell:B cell adhesion process involving integrins, SLAM-associated protein, and CD84. | Q33695371 | ||
| V‐region gene analysis of locally defined synovial B and plasma cells reveals selected B cell expansion and accumulation of plasma cell clones in rheumatoid arthritis | Q33706440 | ||
| Intragraft expression of the IL-10 gene is up-regulated in renal protocol biopsies with early interstitial fibrosis, tubular atrophy, and subclinical rejection | Q33745148 | ||
| Chemokines and cell migration in secondary lymphoid organs | Q33807114 | ||
| Ectopic B-cell clusters that infiltrate transplanted human kidneys are clonal | Q33849715 | ||
| IL-21 and IL-6 are critical for different aspects of B cell immunity and redundantly induce optimal follicular helper CD4 T cell (Tfh) differentiation | Q33851778 | ||
| Development of peripheral lymphoid organs and natural killer cells depends on the helix-loop-helix inhibitor Id2. | Q33854381 | ||
| The extent of affinity maturation differs between the memory and antibody-forming cell compartments in the primary immune response | Q33886727 | ||
| In vivo regulation of Bcl6 and T follicular helper cell development | Q33936471 | ||
| Co-stimulation and selection for T-cell help for germinal centres: the role of CD28 and OX40. | Q33953188 | ||
| Cell distance mapping identifies functional T follicular helper cells in inflamed human renal tissue | Q34030907 | ||
| Lymphoid neogenesis in chronic rejection: evidence for a local humoral alloimmune response | Q34078561 | ||
| Fibroblastic reticular cells of the lymph node are required for retention of resting but not activated CD8+ T cells | Q34082904 | ||
| Type-I interferons suppress microglial production of the lymphoid chemokine, CXCL13. | Q34083294 | ||
| ProxTom lymphatic vessel reporter mice reveal Prox1 expression in the adrenal medulla, megakaryocytes, and platelets | Q34152157 | ||
| The development of inducible bronchus-associated lymphoid tissue depends on IL-17. | Q34191942 | ||
| Extrafollicular antibody responses | Q34212117 | ||
| Regulation of the germinal center reaction by Foxp3+ follicular regulatory T cells | Q34222672 | ||
| Germinal centers | Q34245271 | ||
| Cloning and expression analysis of the murine lymphotoxin beta gene. | Q34317868 | ||
| B cell homeostasis and follicle confines are governed by fibroblastic reticular cells | Q34383642 | ||
| The role of ICOS in the CXCR5+ follicular B helper T cell maintenance in vivo | Q34440540 | ||
| Lymphotoxin alpha/beta and tumor necrosis factor are required for stromal cell expression of homing chemokines in B and T cell areas of the spleen | Q34488105 | ||
| Microbiota-induced tertiary lymphoid tissues aggravate inflammatory disease in the absence of RORgamma t and LTi cells | Q34501407 | ||
| Toll-like receptor 7 and TLR9 dictate autoantibody specificity and have opposing inflammatory and regulatory roles in a murine model of lupus. | Q34566135 | ||
| Interaction of mature CD3+CD4+ T cells with dendritic cells triggers the development of tertiary lymphoid structures in the thyroid. | Q34568588 | ||
| Systemic inflammation in progressive multiple sclerosis involves follicular T-helper, Th17- and activated B-cells and correlates with progression | Q34613311 | ||
| Molecular mechanisms of lymphangiogenesis in health and disease | Q34710547 | ||
| Development of secondary lymphoid organs | Q34764895 | ||
| A fundamental role for interleukin-21 in the generation of T follicular helper cells | Q34792475 | ||
| Salivary glands act as mucosal inductive sites via the formation of ectopic germinal centers after site-restricted MCMV infection | Q34813263 | ||
| In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. I. The architecture and dynamics of responding cell populations | Q34885732 | ||
| Broad diversity of neutralizing antibodies isolated from memory B cells in HIV-infected individuals | Q34962766 | ||
| Stromal cell contributions to the homeostasis and functionality of the immune system. | Q34994909 | ||
| Unique ectopic lymph node-like structures present in human primary colorectal carcinoma are identified by immune gene array profiling | Q35070183 | ||
| Type I interferon production by tertiary lymphoid tissue developing in response to 2,6,10,14-tetramethyl-pentadecane (pristane) | Q35088161 | ||
| Organogenesis of lymphoid tissues | Q35096187 | ||
| Class-switched memory B cells remodel BCRs within secondary germinal centers | Q35097102 | ||
| Follicular dendritic cells: dynamic antigen libraries. | Q35191870 | ||
| Are follicular dendritic cells really good for nothing? | Q35209481 | ||
| A dynamic T cell-limited checkpoint regulates affinity-dependent B cell entry into the germinal center | Q35213561 | ||
| Foxp3+ follicular regulatory T cells control the germinal center response. | Q35239023 | ||
| Circulating tumour necrosis factor alpha and soluble tumour necrosis factor receptors in patients with different patterns of rheumatoid synovitis | Q35552625 | ||
| Chemokines in innate and adaptive host defense: basic chemokinese grammar for immune cells | Q35698582 | ||
| Germinal center B cell and T follicular helper cell development initiates in the interfollicular zone | Q35758747 | ||
| Lymphoid tissue homing chemokines are expressed in chronic inflammation | Q35810009 | ||
| A germinal center-independent pathway generates unswitched memory B cells early in the primary response | Q35825984 | ||
| Ectopic lymphoid neogenesis is strongly associated with activation of the IL-23 pathway in rheumatoid synovitis | Q35834582 | ||
| A conduit system distributes chemokines and small blood-borne molecules through the splenic white pulp | Q42109460 | ||
| Clonal selection in the germinal centre by regulated proliferation and hypermutation | Q42185336 | ||
| Lymph node stromal cells negatively regulate antigen-specific CD4+ T cell responses | Q42206223 | ||
| Dynamic signaling by T follicular helper cells during germinal center B cell selection. | Q42406102 | ||
| Mature follicular dendritic cell networks depend on expression of lymphotoxin beta receptor by radioresistant stromal cells and of lymphotoxin beta and tumor necrosis factor by B cells | Q42753323 | ||
| Differentiation of germinal center B cells into plasma cells is initiated by high-affinity antigen and completed by Tfh cells | Q43097047 | ||
| Multiple layers of B cell memory with different effector functions | Q43255281 | ||
| High endothelial venule reporter mice to probe regulation of lymph node vasculature | Q43408041 | ||
| Neogenesis of lymphoid structures and antibody responses occur in human melanoma metastases. | Q43785551 | ||
| Role of antigen receptor affinity in T cell-independent antibody responses in vivo | Q43918933 | ||
| Distinct role of surface lymphotoxin expressed by B cells in the organization of secondary lymphoid tissues | Q44158648 | ||
| Autoimmune disease and impaired uptake of apoptotic cells in MFG-E8-deficient mice | Q44904989 | ||
| Germinal center dark and light zone organization is mediated by CXCR4 and CXCR5. | Q44999948 | ||
| Follicular dendritic cells and B cell costimulation. | Q45093231 | ||
| Banff 2013 meeting report: inclusion of c4d-negative antibody-mediated rejection and antibody-associated arterial lesions | Q45342440 | ||
| The 2013 International Society for Heart and Lung Transplantation Working Formulation for the standardization of nomenclature in the pathologic diagnosis of antibody-mediated rejection in heart transplantation. | Q45987277 | ||
| The expression of B-cell activating factor belonging to tumor necrosis factor superfamily (BAFF) significantly correlated with C4D in kidney allograft rejection | Q46105901 | ||
| B cells in cluster or in a scattered pattern do not correlate with clinical outcome of renal allograft rejection | Q46350414 | ||
| Differing activities of homeostatic chemokines CCL19, CCL21, and CXCL12 in lymphocyte and dendritic cell recruitment and lymphoid neogenesis. | Q46655434 | ||
| The lymphotoxin beta receptor controls organogenesis and affinity maturation in peripheral lymphoid tissues | Q47713235 | ||
| Visualization of specific B and T lymphocyte interactions in the lymph node | Q47892330 | ||
| Inflammation recapitulates the ontogeny of lymphoid stromal cells | Q47976120 | ||
| Follicular Dendritic Cell Activation by TLR Ligands Promotes Autoreactive B Cell Responses. | Q47995140 | ||
| Integration of Th17- and Lymphotoxin-Derived Signals Initiates Meningeal-Resident Stromal Cell Remodeling to Propagate Neuroinflammation. | Q49130159 | ||
| Fibroblastic reticular cells in lymph nodes regulate the homeostasis of naive T cells. | Q50144852 | ||
| The transcriptional repressor Bcl-6 directs T follicular helper cell lineage commitment. | Q50736370 | ||
| The composition of ectopic lymphoid structures suggests involvement of a local immune response in cardiac allograft vasculopathy. | Q50753444 | ||
| Follicular T-helper cell recruitment governed by bystander B cells and ICOS-driven motility. | Q50903417 | ||
| Characterization of chemokines and adhesion molecules associated with T cell presence in tertiary lymphoid structures in human lung cancer. | Q50993488 | ||
| Human solid tumors contain high endothelial venules: association with T- and B-lymphocyte infiltration and favorable prognosis in breast cancer. | Q50996147 | ||
| Intracerebral expression of CXCL13 and BAFF is accompanied by formation of lymphoid follicle-like structures in the meninges of mice with relapsing experimental autoimmune encephalomyelitis. | Q51027456 | ||
| Intragraft Th17 infiltrate promotes lymphoid neogenesis and hastens clinical chronic rejection. | Q51060341 | ||
| The role of intrapulmonary de novo lymphoid tissue in obliterative bronchiolitis after lung transplantation. | Q51956487 | ||
| Tertiary lymphoid tissues generate effector and memory T cells that lead to allograft rejection. | Q51976995 | ||
| Distinct activities of stromal cells involved in the organogenesis of lymph nodes and Peyer's patches. | Q51981354 | ||
| Ectopic lymphoid-organ development occurs through interleukin 7-mediated enhanced survival of lymphoid-tissue-inducer cells. | Q51985115 | ||
| Generation of migratory antigen-specific plasma blasts and mobilization of resident plasma cells in a secondary immune response. | Q51996837 | ||
| CD4(+)CD3(-) accessory cells costimulate primed CD4 T cells through OX40 and CD30 at sites where T cells collaborate with B cells. | Q52007792 | ||
| Neonatal and adult CD4+ CD3- cells share similar gene expression profile, and neonatal cells up-regulate OX40 ligand in response to TL1A (TNFSF15). | Q52009391 | ||
| Lifetime of plasma cells in the bone marrow. | Q52042101 | ||
| Adhesion through the LFA-1 (CD11a/CD18)-ICAM-1 (CD54) and the VLA-4 (CD49d)-VCAM-1 (CD106) pathways prevents apoptosis of germinal center B cells. | Q52058256 | ||
| Induction of secondary and tertiary lymphoid structures in the skin. | Q52085787 | ||
| Control of the T follicular helper-germinal center B-cell axis by CD8⁺ regulatory T cells limits atherosclerosis and tertiary lymphoid organ development. | Q52656274 | ||
| Description of B lymphocytes and plasma cells, complement, and chemokines/receptors in acute liver allograft rejection. | Q52943871 | ||
| Chemotactic responsiveness toward ligands for CXCR3 and CXCR4 is regulated on plasma blasts during the time course of a memory immune response. | Q52956500 | ||
| Molecular heterogeneity in acute renal allograft rejection identified by DNA microarray profiling. | Q53924174 | ||
| Potential involvement of IL-22 and IL-22-producing cells in the inflamed salivary glands of patients with Sjogren's syndrome. | Q54344928 | ||
| A BAFF/APRIL-dependent TLR3-stimulated pathway enhances the capacity of rheumatoid synovial fibroblasts to induce AID expression and Ig class-switching in B cells. | Q54356847 | ||
| B cell survival in intragraft tertiary lymphoid organs after rituximab therapy. | Q54528998 | ||
| M1 macrophages act as LTβR-independent lymphoid tissue inducer cells during atherosclerosis-related lymphoid neogenesis. | Q54541923 | ||
| Presence of B Cells in Tertiary Lymphoid Structures Is Associated with a Protective Immunity in Patients with Lung Cancer | Q56965679 | ||
| Peripheral antigen display by lymph node stroma promotes T cell tolerance to intestinal self | Q57232929 | ||
| Anti-Inflammatory Activity of Immunoglobulin G Resulting from Fc Sialylation | Q57253538 | ||
| High CXCL10 Expression in Rejected Kidneys and Predictive Role of Pretransplant Serum CXCL10 for Acute Rejection And Chronic Allograft Nephropathy | Q57582463 | ||
| Mechanism of antigen-driven selection in germinal centres | Q59072211 | ||
| Chronic Rejection Triggers the Development of an Aggressive Intragraft Immune Response through Recapitulation of Lymphoid Organogenesis | Q59387561 | ||
| Donor CD4 T Cells Contribute to Cardiac Allograft Vasculopathy by Providing Help for Autoantibody Production | Q60056590 | ||
| Identification of Bcl-6-dependent follicular helper NKT cells that provide cognate help for B cell responses | Q60311662 | ||
| Function of CD4+CD3- cells in relation to B- and T-zone stroma in spleen | Q63346578 | ||
| Production of tumor necrosis factor (TNF-alpha) and lymphotoxin (TNF-beta) by murine pre-B and B cell lymphomas | Q68760848 | ||
| Antigen-specific B cells efficiently present low doses of antigen for induction of T cell proliferation | Q68934632 | ||
| Differential regulation of lymphotoxin (LT), lymphotoxin-beta (LT-beta), and TNF-alpha in murine T cell clones activated through the TCR | Q72363560 | ||
| Isolated lymphoid follicle formation is inducible and dependent upon lymphotoxin-sufficient B lymphocytes, lymphotoxin beta receptor, and TNF receptor I function | Q73419615 | ||
| Developing lymph nodes collect CD4+CD3- LTbeta+ cells that can differentiate to APC, NK cells, and follicular cells but not T or B cells | Q73838320 | ||
| Lymphoid neogenesis in rheumatoid synovitis | Q74147962 | ||
| Inflamed kidneys of NZB / W mice are a major site for the homeostasis of plasma cells | Q74460576 | ||
| Initiation of NALT organogenesis is independent of the IL-7R, LTbetaR, and NIK signaling pathways but requires the Id2 gene and CD3(-)CD4(+)CD45(+) cells | Q74548133 | ||
| Ectopic expression of the B cell-attracting chemokine BCA-1 (CXCL13) on endothelial cells and within lymphoid follicles contributes to the establishment of germinal center-like structures in Sjögren's syndrome | Q77179303 | ||
| Intramolecular and intermolecular spreading during the course of organ allograft rejection | Q77488397 | ||
| Different cytokines induce surface lymphotoxin-alphabeta on IL-7 receptor-alpha cells that differentially engender lymph nodes and Peyer's patches | Q78651212 | ||
| Quilty effect has the features of lymphoid neogenesis and shares CXCL13-CXCR5 pathway with recurrent acute cardiac rejections | Q79296607 | ||
| B cell-mediated antigen presentation is required for the pathogenesis of acute cardiac allograft rejection | Q79370183 | ||
| Expression of the chemokine receptor CCR1 in human renal allografts | Q79770897 | ||
| Graded expression of interferon regulatory factor-4 coordinates isotype switching with plasma cell differentiation | Q80139485 | ||
| Lymphotoxin beta-mediated stimulation of synoviocytes in rheumatoid arthritis | Q80330562 | ||
| Lymphoid neogenesis in murine cardiac allografts undergoing chronic rejection | Q81395004 | ||
| Adaptive immune responses are dispensable for isolated lymphoid follicle formation: antigen-naive, lymphotoxin-sufficient B lymphocytes drive the formation of mature isolated lymphoid follicles | Q81672214 | ||
| OX40 ligand and CD30 ligand are expressed on adult but not neonatal CD4+CD3- inducer cells: evidence that IL-7 signals regulate CD30 ligand but not OX40 ligand expression | Q81767161 | ||
| Glomerular inflammation in renal allografts biopsies after the first year: cell types and relationship with antibody-mediated rejection and graft outcome | Q82267596 | ||
| Germinal centers | Q83884068 | ||
| Stromal activation and formation of lymphoid-like stroma in chronic lung allograft dysfunction | Q83930980 | ||
| B cells and plasma cells in coronaries of chronically rejected cardiac transplants | Q84047305 | ||
| Guidance of B cells by the orphan G protein-coupled receptor EBI2 shapes humoral immune responses | Q84250521 | ||
| Blocking lymphotoxin signaling abrogates the development of ectopic lymphoid tissue within cardiac allografts and inhibits effector antibody responses | Q84958034 | ||
| Establishment of early lymphoid organ infrastructure in transplanted tumors mediated by local production of lymphotoxin alpha and in the combined absence of functional B and T cells | Q38462714 | ||
| Early up-regulation of macrophages and myofibroblasts: a new marker for development of chronic renal allograft rejection | Q38496170 | ||
| Regulation of germinal center responses, memory B cells and plasma cell formation-an update | Q38707784 | ||
| T follicular regulatory cells | Q38810922 | ||
| T follicular helper and T follicular regulatory cells have different TCR specificity. | Q38827181 | ||
| T follicular helper cells in human autoimmunity | Q38944810 | ||
| Germinal Center B Cell Dynamics | Q38960786 | ||
| Lymphoid Neogenesis and Tertiary Lymphoid Organs in Transplanted Organs. | Q39084586 | ||
| Germinal centers: programmed for affinity maturation and antibody diversification | Q39088982 | ||
| High Endothelial Venules and Other Blood Vessels: Critical Regulators of Lymphoid Organ Development and Function | Q39143550 | ||
| Plasma cell and memory B cell differentiation from the germinal center. | Q39188175 | ||
| Effects of CD20+ B-cell infiltration into allografts on kidney transplantation outcomes: a systematic review and meta-analysis | Q39246422 | ||
| Stromal cells direct local differentiation of regulatory dendritic cells | Q39501106 | ||
| HUMORAL IMMUNITY. T cell help controls the speed of the cell cycle in germinal center B cells. | Q39553791 | ||
| Short-circuiting long-lived humoral immunity by the heightened engagement of CD40. | Q39737614 | ||
| Lymphotoxin-Dependent B Cell-FRC Crosstalk Promotes De Novo Follicle Formation and Antibody Production following Intestinal Helminth Infection. | Q39781756 | ||
| Interleukin 17 acts in synergy with B cell-activating factor to influence B cell biology and the pathophysiology of systemic lupus erythematosus. | Q39844668 | ||
| Humoral immunity. Apoptosis and antigen affinity limit effector cell differentiation of a single naïve B cell | Q40019887 | ||
| Expression of B cell and immunoglobulin transcripts is a feature of inflammation in late allografts | Q40097494 | ||
| Opposing impact of B cell-intrinsic TLR7 and TLR9 signals on autoantibody repertoire and systemic inflammation | Q40173384 | ||
| B cells extract and present immobilized antigen: implications for affinity discrimination | Q40387022 | ||
| Regulated selection of germinal-center cells into the memory B cell compartment. | Q40682557 | ||
| Follicular Helper T Cells | Q40780566 | ||
| B cells acquire antigen from target cells after synapse formation | Q40803432 | ||
| T follicular helper cells have distinct modes of migration and molecular signatures in naive and memory immune responses. | Q41117519 | ||
| CD40 ligation induces lymphotoxin alpha gene expression in human B cells | Q41425894 | ||
| BLC expression in pancreatic islets causes B cell recruitment and lymphotoxin-dependent lymphoid neogenesis. | Q41740089 | ||
| Inhibition of follicular T-helper cells by CD8(+) regulatory T cells is essential for self tolerance. | Q41870591 | ||
| Thyroid autoimmune disease: demonstration of thyroid antigen-specific B cells and recombination-activating gene expression in chemokine-containing active intrathyroidal germinal centers | Q41873772 | ||
| Inflammation-induced lymphangiogenesis in the cornea arises from CD11b-positive macrophages | Q41887679 | ||
| Follicular regulatory T cells expressing Foxp3 and Bcl-6 suppress germinal center reactions | Q41911767 | ||
| Compromised OX40 function in CD28-deficient mice is linked with failure to develop CXC chemokine receptor 5-positive CD4 cells and germinal centers. | Q42006087 | ||
| Molecular basis for hematopoietic/mesenchymal interaction during initiation of Peyer's patch organogenesis. | Q42076869 | ||
| P921 | main subject | B-cell | Q188930 |
| tertiary lymphoid organ | Q108017266 | ||
| P304 | page(s) | 1639 | |
| P577 | publication date | 2017-11-23 | |
| P1433 | published in | Frontiers in Immunology | Q27723748 |
| P1476 | title | Spoiling for a Fight: B Lymphocytes As Initiator and Effector Populations within Tertiary Lymphoid Organs in Autoimmunity and Transplantation | |
| P478 | volume | 8 |
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