CAR-T Cell–Mediated B-Cell Depletion in Central Nervous System Autoimmunity. Issue 2 (19th March 2023)
- Record Type:
- Journal Article
- Title:
- CAR-T Cell–Mediated B-Cell Depletion in Central Nervous System Autoimmunity. Issue 2 (19th March 2023)
- Main Title:
- CAR-T Cell–Mediated B-Cell Depletion in Central Nervous System Autoimmunity
- Authors:
- Gupta, Sasha
Simic, Milos
Sagan, Sharon A.
Shepherd, Chanelle
Duecker, Jason
Sobel, Raymond A.
Dandekar, Ravi
Wu, Gregory F.
Wu, Wesley
Pak, John E.
Hauser, Stephen L.
Lim, Wendell
Wilson, Michael R.
Zamvil, Scott S. - Abstract:
- Abstract : Background and Objectives: Anti-CD20 monoclonal antibody (mAb) B-cell depletion is a remarkably successful multiple sclerosis (MS) treatment. Chimeric antigen receptor (CAR)-T cells, which target antigens in a non-major histocompatibility complex (MHC)–restricted manner, can penetrate tissues more thoroughly than mAbs. However, a previous study indicated that anti-CD19 CAR-T cells can paradoxically exacerbate experimental autoimmune encephalomyelitis (EAE) disease. We tested anti-CD19 CAR-T cells in a B-cell–dependent EAE model that is responsive to anti-CD20 B-cell depletion similar to the clinical benefit of anti-CD20 mAb treatment in MS. Methods: Anti-CD19 CAR-T cells or control cells that overexpressed green fluorescent protein were transferred into C57BL/6 mice pretreated with cyclophosphamide (Cy). Mice were immunized with recombinant human (rh) myelin oligodendrocyte protein (MOG), which causes EAE in a B-cell–dependent manner. Mice were evaluated for B-cell depletion, clinical and histologic signs of EAE, and immune modulation. Results: Clinical scores and lymphocyte infiltration were reduced in mice treated with either anti-CD19 CAR-T cells with Cy or control cells with Cy, but not with Cy alone. B-cell depletion was observed in peripheral lymphoid tissue and in the CNS of mice treated with anti-CD19 CAR-T cells with Cy pretreatment. Th1 or Th17 populations did not differ in anti-CD19 CAR-T cell, control cell-treated animals, or Cy alone. Discussion: InAbstract : Background and Objectives: Anti-CD20 monoclonal antibody (mAb) B-cell depletion is a remarkably successful multiple sclerosis (MS) treatment. Chimeric antigen receptor (CAR)-T cells, which target antigens in a non-major histocompatibility complex (MHC)–restricted manner, can penetrate tissues more thoroughly than mAbs. However, a previous study indicated that anti-CD19 CAR-T cells can paradoxically exacerbate experimental autoimmune encephalomyelitis (EAE) disease. We tested anti-CD19 CAR-T cells in a B-cell–dependent EAE model that is responsive to anti-CD20 B-cell depletion similar to the clinical benefit of anti-CD20 mAb treatment in MS. Methods: Anti-CD19 CAR-T cells or control cells that overexpressed green fluorescent protein were transferred into C57BL/6 mice pretreated with cyclophosphamide (Cy). Mice were immunized with recombinant human (rh) myelin oligodendrocyte protein (MOG), which causes EAE in a B-cell–dependent manner. Mice were evaluated for B-cell depletion, clinical and histologic signs of EAE, and immune modulation. Results: Clinical scores and lymphocyte infiltration were reduced in mice treated with either anti-CD19 CAR-T cells with Cy or control cells with Cy, but not with Cy alone. B-cell depletion was observed in peripheral lymphoid tissue and in the CNS of mice treated with anti-CD19 CAR-T cells with Cy pretreatment. Th1 or Th17 populations did not differ in anti-CD19 CAR-T cell, control cell-treated animals, or Cy alone. Discussion: In contrast to previous data showing that anti-CD19 CAR-T cell treatment exacerbated EAE, we observed that anti-CD19 CAR-T cells ameliorated EAE. In addition, anti-CD19 CAR-T cells thoroughly depleted B cells in peripheral tissues and in the CNS. However, the clinical benefit occurred independently of antigen specificity or B-cell depletion. … (more)
- Is Part Of:
- Neurology. Volume 10:Issue 2(2023)
- Journal:
- Neurology
- Issue:
- Volume 10:Issue 2(2023)
- Issue Display:
- Volume 10, Issue 2 (2023)
- Year:
- 2023
- Volume:
- 10
- Issue:
- 2
- Issue Sort Value:
- 2023-0010-0002-0000
- Page Start:
- Page End:
- Publication Date:
- 2023-03-19
- Subjects:
- Neuroimmunology -- Periodicals
Neurology -- Periodicals
616.8 - Journal URLs:
- http://nn.neurology.org/ ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1212/NXI.0000000000200080 ↗
- Languages:
- English
- ISSNs:
- 2332-7812
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.502260
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