Post-doctoral fellowship -- B cell & antibody response in tuberculosis
New Jersey Medical School, Rutgers
See the full job description on jobRxiv: https://jobrxiv.org/job/new-jersey-medical-school-rutgers-27778-post-doctoral-fellowship-b-cell-antibody-response-in-tuberculosis/
#Antibody #antigenpresentation #bcells #cytokines #Inflammation #Science...
https://jobrxiv.org/job/new-jersey-medical-school-rutgers-27778-post-doctoral-fellowship-b-cell-antibody-response-in-tuberculosis/?fsp_sid=9993
Post-doctoral fellowship -- B cell & antibody response in tuberculosis
New Jersey Medical School, Rutgers
See the full job description on jobRxiv: https://jobrxiv.org/job/new-jersey-medical-school-rutgers-27778-post-doctoral-fellowship-b-cell-antibody-response-in-tuberculosis/
#Antibody #antigenpresentation #bcells #cytokines #Inflammation #Science...
https://jobrxiv.org/job/new-jersey-medical-school-rutgers-27778-post-doctoral-fellowship-b-cell-antibody-response-in-tuberculosis/?fsp_sid=9489
" The insights derived from this analysis do not only support a CD19 CAR T cell-mediated reset of the memory B cell compartment, but also the parallel inhibition of the interferon signature
in #monocytes and #Tcells of #SLE patients"
https://insight.jci.org/articles/view/179433
Striking that this apparently works better in getting rid of certain memory #Bcells than anti-CD20 antibodies.
Plenary Speaker Profile: Meet Dr. Oliver Harrison, Assistant Member at the Benaroya Research Institute and Affiliate Assistant Professor at the University of Washington who will speak about antigen-level resolution of commensal-specific B cell responses at #HavingIMPACTT2024
#microbiome #microbiota #immunology #bcells #antigen #conference #symposium
Researchers discovered that #Bcells play an active role in teaching #Tcells not to attack the body itself. If the "training" fails, #autoimmunediseases such as #neuromyelitis optica can develop: http://go.tum.de/562972
📷J. Böttcher, T. Korn
The great thing about high profile moron “experts” making blithe uninformed comments such as “Covid doesn’t really damage the immune system” is it angers people who ACTUALLY know & they come at them with #CovidPapers #Jha
This will be my continuing🧵on anything related to the destruction of #tcells #bcells #ImmuneDysregulation in an attempt to be organized if only for myself🖤
Published January 14, 2022
https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-021-02228-6
In truth just skimmed but my grasp on this in January 2024 is something that would have been impossible for me to understand in 2022 while experiencing my #sarscov2 2nd infection b/c my level of biology was zero & my lack of understanding led me to believe #hybridImmunity would give me 2 years at least. Mind you I never took my mask off except w/my MIL🦃🎄2021
Philip Dettmer “immune” book along w/the incredibly intelligent🧠🧠🧠here🐘&🐦have been invaluable in at least allowing me to read & generally follow along
Basically this study tells me, stay down for 6 months minimum
Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a highly infectious respiratory virus which is responsible for the coronavirus disease 2019 (COVID-19) pandemic. It is increasingly clear that recovered individuals, even those who had mild COVID-19, can suffer from persistent symptoms for many months after infection, a condition referred to as “long COVID”, post-acute sequelae of COVID-19 (PASC), post-acute COVID-19 syndrome, or post COVID-19 condition. However, despite the plethora of research on COVID-19, relatively little is known about the molecular underpinnings of these long-term effects. Methods We have undertaken an integrated analysis of immune responses in blood at a transcriptional, cellular, and serological level at 12, 16, and 24 weeks post-infection (wpi) in 69 patients recovering from mild, moderate, severe, or critical COVID-19 in comparison to healthy uninfected controls. Twenty-one of these patients were referred to a long COVID clinic and > 50% reported ongoing symptoms more than 6 months post-infection. Results Anti-Spike and anti-RBD IgG responses were largely stable up to 24 wpi and correlated with disease severity. Deep immunophenotyping revealed significant differences in multiple innate (NK cells, LD neutrophils, CXCR3+ monocytes) and adaptive immune populations (T helper, T follicular helper, and regulatory T cells) in convalescent individuals compared to healthy controls, which were most strongly evident at 12 and 16 wpi. RNA sequencing revealed significant perturbations to gene expression in COVID-19 convalescents until at least 6 months post-infection. We also uncovered significant differences in the transcriptome at 24 wpi of convalescents who were referred to a long COVID clinic compared to those who were not. Conclusions Variation in the rate of recovery from infection at a cellular and transcriptional level may explain the persistence of symptoms associated with long COVID in some individuals.