AI Article Synopsis

  • The procedure describes a method for enriching and growing CD4+ T cells, potentially useful for HIV-1 immunotherapy, using anti-CD3 and anti-CD28 coated beads for stimulation.
  • The process begins by isolating PBMCs from apheresis products, removing monocytes/macrophages, and depleting B and CD8+ cells, resulting in over 80% CD4+ cells.
  • After culturing these enriched cells for 14 days, cell numbers increased by 37 times, and viral load decreased significantly without using antiretroviral agents, highlighting the method’s efficiency for HIV-1 positive donors.

Article Abstract

We describe a procedure for large-scale enrichment, growth, and harvesting CD4+ T cells. This method may be effective for HIV-1 immunotherapy, as the mode of stimulation, with anti-CD3 plus anti-CD28 coated beads (CD3/CD28 beads) induces a potent antiviral effect. PBMC were obtained by density gradient centrifugation of an apheresis product. Monocytes/macrophages were removed by incubating PBMC with beads coated with IgG. The cells were then magnetically depleted of B cells and CD8+ cells with mouse anti-CD20 and anti-CD8 MAbs and sheep antimouse coated beads. The remaining cells were >80% CD4+ and were transferred to gas-permeable bags containing CD3/CD28 beads and cultured in a closed system. After 14 days, the cell number increased an average of 37-fold, and cells were nearly 100% CD4+. Viral load, assessed by DNA PCR for HIV-1 gag, decreased >10-fold during culture in the absence of antiretroviral agents. Removal of CD3/CD28 beads from the cell suspension was accomplished by passing cells plus beads (3-30 x 10(9) cells in 2-12 L) over a MaxSep magnetic separator using gravity-driven flow. The cells were then concentrated to 300 ml in an automated centrifuge. This process allows safe and efficient growth of large numbers of CD4+ T cells from HIV-1+ donors.

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Source
http://dx.doi.org/10.1089/scd.1.1998.7.437DOI Listing

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