Immune Repertoires in Various Dermatologic and Autoimmune Diseases DOI Open Access
Hanna Terhaar, Victoria Jiminez, Ellsworth Grant

и другие.

Genes, Год журнала: 2024, Номер 15(12), С. 1591 - 1591

Опубликована: Дек. 11, 2024

The immune repertoire (IR) is a term that defines the combined unique genetic rearrangements of antigen receptors expressed by B and T lymphocytes. IR determines ability system to identify respond foreign antigens while preserving tolerance host antigens. When disrupted, development autoimmune diseases can occur due attack self-antigens. Recent technical advances in profiling allowed identification common patterns shared antigen-binding sequences diverse array diseases. However, there no current literature date evaluates findings skin inflammatory conditions. In this review, we provide an overview past research various dermatologic Enriching our understanding IRs these conditions critical for pathophysiology behind disease onset progression. Furthermore, B-cell T-cell will help devise therapeutic treatments hopes restoring preventing

Язык: Английский

CAR T-cell therapy in autoimmune diseases: where are we and where are we going? DOI
Marc Scherlinger, Gaëtane Nocturne, Marko Radic

и другие.

The Lancet Rheumatology, Год журнала: 2025, Номер unknown

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

CAR-T cell therapy for juvenile-onset autoimmune diseases: a promising future? DOI Creative Commons

Maurine Jouret,

Sébastien Viel, Benjamin Fournier

и другие.

Arthritis Research & Therapy, Год журнала: 2025, Номер 27(1)

Опубликована: Май 10, 2025

Chimeric antigen receptor (CAR) T-cell therapy targeting B cells has shown promising results, including drug-free remission, in adult-onset autoimmune diseases. Extending this therapeutic approach to the pediatric population, particularly for juvenile diseases, presents an exciting opportunity. However, challenges specific juvenile-onset conditions, such as long-term adverse events, heightened disease activity, and imperative reduce steroid exposure, must be considered. While strategy appears viable these severe limited data available population absence of evidence on cases with a high genetic component, monogenic lupus, represent significant challenges. Most lupus are associated innate immune defects, involvement anomalies remains poorly understood. In review, we examine potential indications, current knowledge, limitations CAR-T cell extending discussion beyond early-onset lupus.

Язык: Английский

Процитировано

0

Early diagnosis of systemic lupus erythematosus DOI Open Access
Martin Aringer, George Βertsias

Rare Disease and Orphan Drugs Journal, Год журнала: 2025, Номер 4(2)

Опубликована: Май 28, 2025

Systemic lupus erythematosus (SLE) poses significant diagnostic challenges. First, it is characterized by a highly variable combination of autoantibodies and wide range possible organ involvement symptoms. Second, no single laboratory test can definitively confirm or exclude the diagnosis. Third, due to low incidence SLE, clinicians must carefully balance considering SLE as potential diagnosis against more common causes similar The joint European League Against Rheumatism/American College Rheumatology (EULAR/ACR) classification criteria provide helpful framework for thinking about diagnosis, although they are not intended use. Nevertheless, several elements - such requirement anti-nuclear antibodies (ANA) positivity an entry point (similar screening test), weighted scoring clinical immunological features, attribution findings only when likely alternative explanation exists highlight principles that also useful in process. Conceptionally, diagnosing be seen three-step process: (1) possibility SLE; (2) systematically collecting evidence diagnosis; (3) making decision based on whether accumulated sufficiently supports refutes This review follows discussing

Язык: Английский

Процитировано

0

Releasing our model T – chimeric antigen receptor (CAR) T-cells for autoimmune indications DOI
Holly Wobma, Joyce C. Chang, Susan E. Prockop

и другие.

Current Opinion in Rheumatology, Год журнала: 2024, Номер unknown

Опубликована: Окт. 24, 2024

Purpose of review This provides an update on the rapidly growing field engineered cellular therapies for autoimmune disorders, primarily focusing clinical experience and correlative studies with chimeric antigen receptor (CAR) T-cells. Recent findings To date, two case series describing treatment CAR T-cell therapy systemic lupus erythematosus (SLE) suggest that drug-free remission can be sustained in patients previously treatment-refractory disease. The outcomes these are similar, despite use different constructs lymphodepletion regimens. Although it is not yet clear whether described have truly been cured, majority remissions remained durable up to last follow-up at 1–2 years from treatment. Meanwhile, mechanistic providing a window into how transient B-cell depletion mediates lasting benefit. With encouraging data SLE, T-cells other novel B-cell-depleting agents (e.g. bispecific engagers) now being evaluated as conditions, goal response. Summary reports highlight promising strategy conditions; however, there still limited experience, better insight this therapeutic approach expected emerge rapidly.

Язык: Английский

Процитировано

1

Harnessing the potential of CAR-T cell in lupus treatment: From theory to practice DOI Creative Commons
Tamim Alsuliman, Zora Marjanovic, Doron Rimar

и другие.

Autoimmunity Reviews, Год журнала: 2024, Номер 23(12), С. 103687 - 103687

Опубликована: Ноя. 10, 2024

Язык: Английский

Процитировано

0

CAR T cells in autoimmune disease: On the road to remission DOI
Georg Schett, Carl H. June

Immunity, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 1, 2024

Язык: Английский

Процитировано

0

Proteomic analysis of B cells in peripheral lymphatic system reveals the dynamics during the systemic lupus erythematosus progression DOI Creative Commons
Liming Sun, Yuanyuan Yin, Yuqing Cao

и другие.

Biophysics Reports, Год журнала: 2024, Номер 11(2), С. 129 - 129

Опубликована: Ноя. 19, 2024

In this study, we conducted a comprehensive proteomic analysis of B cells from the spleen, mesenteric lymph nodes (mLN), and peripheral blood mononuclear (PBMC) in time-course model systemic lupus erythematosus (SLE) using female MRL/lpr mice. By combining fluorescence-activated cell sorting (FACS) 4D-Data-Independent Acquisition (4D-DIA) mass spectrometry, quantified nearly 8000 proteins, identifying significant temporal tissue-specific changes during SLE progression. PBMC-derived exhibited early alterations by Week 9, while spleen-derived showed similar 12. We identified key regulatory including BAFF, BAFFR, NFKB2, involved survival activation, as well novel markers such CD11c CD117, which have previously been associated with other immune cells. The study highlights dynamic reprogramming proteomes across different tissues, distinct contributions to pathogenesis, providing valuable insights into molecular mechanisms underlying dysregulation lupus. These findings offer potential therapeutic targets biomarkers for SLE.

Язык: Английский

Процитировано

0

Immune Repertoires in Various Dermatologic and Autoimmune Diseases DOI Open Access
Hanna Terhaar, Victoria Jiminez, Ellsworth Grant

и другие.

Genes, Год журнала: 2024, Номер 15(12), С. 1591 - 1591

Опубликована: Дек. 11, 2024

The immune repertoire (IR) is a term that defines the combined unique genetic rearrangements of antigen receptors expressed by B and T lymphocytes. IR determines ability system to identify respond foreign antigens while preserving tolerance host antigens. When disrupted, development autoimmune diseases can occur due attack self-antigens. Recent technical advances in profiling allowed identification common patterns shared antigen-binding sequences diverse array diseases. However, there no current literature date evaluates findings skin inflammatory conditions. In this review, we provide an overview past research various dermatologic Enriching our understanding IRs these conditions critical for pathophysiology behind disease onset progression. Furthermore, B-cell T-cell will help devise therapeutic treatments hopes restoring preventing

Язык: Английский

Процитировано

0