| Q34129905 | A Chlamydia trachomatis-specific Th2 clone does not provide protection against a genital infection and displays reduced trafficking to the infected genital mucosa |
| Q33606828 | A MyD88-dependent early IL-17 production protects mice against airway infection with the obligate intracellular pathogen Chlamydia muridarum |
| Q35214742 | A limited role for antibody in protective immunity induced by rCPAF and CpG vaccination against primary genital Chlamydia muridarum challenge. |
| Q33716068 | A live and inactivated Chlamydia trachomatis mouse pneumonitis strain induces the maturation of dendritic cells that are phenotypically and immunologically distinct |
| Q36445638 | A predominant role for antibody in acquired immunity to chlamydial genital tract reinfection |
| Q35471373 | A re-evaluation of the role of B cells in protective immunity to Chlamydia infection |
| Q42537466 | B Cell Depletion With an Anti-CD20 Antibody Enhances Alloreactive Memory T Cell Responses After Transplantation |
| Q93052209 | B Cell and CD4 T Cell Interactions Promote Development of Atherosclerosis |
| Q35816029 | B Lymphocytes Are Required during the Early Priming of CD4+ T Cells for Clearance of Pneumocystis Infection in Mice |
| Q37264863 | B cell production of tumor necrosis factor in response to Pneumocystis murina infection in mice |
| Q36371044 | B cell-dependent T cell responses: IgM antibodies are required to elicit contact sensitivity |
| Q35034215 | B cells enhance antigen-specific CD4 T cell priming and prevent bacteria dissemination following Chlamydia muridarum genital tract infection. |
| Q42409134 | B cells help alloreactive T cells differentiate into memory T cells. |
| Q28083170 | B cells responses and cytokine production are regulated by their immune microenvironment |
| Q34259955 | B-cell-deficient mice show an exacerbated inflammatory response in a model of Chlamydophila abortus infection. |
| Q35679647 | Bioinformatic Analysis of Chlamydia trachomatis Polymorphic Membrane Proteins PmpE, PmpF, PmpG and PmpH as Potential Vaccine Antigens |
| Q37844159 | CD43-, but not CD43+, IL-10-producing CD1dhiCD5+ B cells suppress type 1 immune responses during Chlamydia muridarum genital tract infection |
| Q40403750 | Characterization and development of T-Cell immune responses in B-cell-deficient (Igh-6(-/-)) mice with Salmonella enterica serovar Typhimurium infection |
| Q34103774 | Chlamydia trachomatis control requires a vaccine |
| Q34144392 | Clearance of Citrobacter rodentium requires B cells but not secretory immunoglobulin A (IgA) or IgM antibodies. |
| Q34119773 | Dendritic cells pulsed with a recombinant chlamydial major outer membrane protein antigen elicit a CD4(+) type 2 rather than type 1 immune response that is not protective |
| Q37142202 | Developing idiotype vaccines for lymphoma: from preclinical studies to phase III clinical trials |
| Q34684829 | Differential and site specific impact of B cells in the protective immune response to Mycobacterium tuberculosis in the mouse |
| Q37872443 | Fc receptor regulation of protective immunity against Chlamydia trachomatis |
| Q35541507 | Gene expression profiling in acute allograft rejection: challenging the immunologic constant of rejection hypothesis |
| Q33565893 | Genetic variation in Chlamydia trachomatis and their hosts: impact on disease severity and tissue tropism |
| Q37383963 | How B cells shape the immune response against Mycobacterium tuberculosis |
| Q35665366 | Identifying a role for Toll-like receptor 3 in the innate immune response to Chlamydia muridarum infection in murine oviduct epithelial cells |
| Q37837985 | IgA modulates respiratory dysfunction as a sequela to pulmonary chlamydial infection as neonates |
| Q34002939 | Igh-6(-/-) (B-cell-deficient) mice fail to mount solid acquired resistance to oral challenge with virulent Salmonella enterica serovar typhimurium and show impaired Th1 T-cell responses to Salmonella antigens |
| Q34005295 | Immunity to murine Chlamydia trachomatis genital tract reinfection involves B cells and CD4(+) T cells but not CD8(+) T cells |
| Q34685461 | Immunization with a MOMP-based vaccine protects mice against a pulmonary Chlamydia challenge and identifies a disconnection between infection and pathology |
| Q37874602 | Immunological memory in B-cell-deficient mice conveys long-lasting protection against genital tract infection with Chlamydia trachomatis by rapid recruitment of T cells |
| Q37836040 | Immunopathogenesis of Chlamydial Infections |
| Q34002527 | Importance of B cells, but not specific antibodies, in primary and secondary protective immunity to the intracellular bacterium Francisella tularensis live vaccine strain |
| Q34006511 | Inflammation and clearance of Chlamydia trachomatis in enteric and nonenteric mucosae |
| Q34760989 | Intranasal vaccination with Chlamydia pneumoniae induces cross-species immunity against genital Chlamydia muridarum challenge in mice |
| Q37129928 | Intravenous Inoculation with Chlamydia muridarum Leads to a Long-Lasting Infection Restricted to the Gastrointestinal Tract |
| Q37867467 | Less inhibition of interferon-gamma to organism growth in host cells may contribute to the high susceptibility of C3H mice to Chlamydia trachomatis lung infection |
| Q37331068 | Modulation of cytokines and transcription factors (T-Bet and GATA3) in CD4 enriched cervical cells of Chlamydia trachomatis infected fertile and infertile women upon stimulation with chlamydial inclusion membrane proteins B and C. |
| Q37135496 | Requirement of B cells for generating CD4+ T cell memory |
| Q34007017 | Resolution of secondary Chlamydia trachomatis genital tract infection in immune mice with depletion of both CD4+ and CD8+ T cells |
| Q36369671 | Splenic T zone development is B cell dependent |
| Q39517769 | Susceptibility to secondary Francisella tularensis live vaccine strain infection in B-cell-deficient mice is associated with neutrophilia but not with defects in specific T-cell-mediated immunity |
| Q61823403 | Systemic mycobacterial infection inhibits antigen-specific immunoglobulin E production, bronchial mucus production and eosinophilic inflammation induced by allergen |
| Q37399047 | Temporal requirements for B cells in the establishment of CD4 T cell memory |
| Q33727953 | The cryptic plasmid is more important for Chlamydia muridarum to colonize the mouse gastrointestinal tract than to infect the genital tract |
| Q44059069 | The genital tract virulence factor pGP3 is essential for Chlamydia muridarum colonization in the gastrointestinal tract |
| Q86299842 | The role of B cells and humoral immunity in Mycobacterium tuberculosis infection |
| Q35039807 | The role of B cells and humoral immunity in Mycobacterium tuberculosis infection |
| Q28075820 | Tissue-Resident T Cells as the Central Paradigm of Chlamydia Immunity |
| Q27010202 | Unraveling effector functions of B cells during infection: the hidden world beyond antibody production |
| Q34352839 | Yes T cells, but three different T cells (alphabeta, gammadelta and NK T cells), and also B-1 cells mediate contact sensitivity |