B cell immunotherapy
A technology of B cells and cells, applied in the field of B cell immunotherapy, can solve the problem of expensive treatment
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[0274] The present invention is described in further detail in the following examples, which are in no way intended to limit the scope of the claimed invention. The accompanying drawings are intended to be considered as an integral part of the specification and description of the invention. All references cited are expressly incorporated by reference for all content described herein. The following examples are offered to illustrate, not limit, the claimed invention.
example 1
[0275] Example 1: Exogenous B Cells Modulate Immune Infiltration and Response
[0276] This example illustrates the large-scale analysis of the molecular impact of B cells in wound healing using isobaric labeling multiplex proteomics.
[0277] Our data show that B cell imposition has a dramatic homeostatic effect on the wound microenvironment, with significant reductions in proteins associated with inflammatory responses and increases in proteins associated with tissue growth and remodeling. By recovering applied exogenous B cells from the wound microenvironment at various time points after application, and examining cell populations by multicolor flow cytometry, we determined that mature naive B cells applied to wounds transitioned to be characterized by expression of CD138 and regulatory phenotypes of the immunomodulatory cytokines IL-10, IL-35, and TGF-β. This Breg-like phenotype was transient, with a peak at day 2 post application. In addition, the phenotype of monocytes...
example 2
[0327] Example 2: B cell treatment improves outcome after TBI
[0328] This example demonstrates that exogenously administered B cells significantly improve post-injury performance in a mouse TBI model.
[0329] Brain contusion results in neurological dysfunction, mediated in part by the inflammatory response to injury. B lymphocytes are dynamic regulators of the immune system and have not been systematically studied in TBI. Using a mouse model of controlled cortical impingement (CCI), we assessed the possible beneficial effects of exogenously applied B cells on histopathological and functional outcomes after TBI. Inject 2×10 mice into the brain parenchyma of the lesion 6 mature naive isogenic splenic B cells, followed by CCI. Control CCI mice received equal amounts of T cells or saline, and sham-injured mice (craniotomy only) were given B cells or saline. The sham-injury group performed similarly on the motor and learning tests. Injured mice administered B cells showed sig...
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