A novel and efficient method to induce allospecific CD8+ memory T lymphocytes

J Clin Lab Anal. 2021 Oct;35(10):e23972. doi: 10.1002/jcla.23972. Epub 2021 Aug 31.

Abstract

The aim of the current study was to establish a simple method for effectively inducing memory T lymphocytes by the intraperitoneal injection of spleen lymphocytes into mice. In total, 75 mice were divided into the following groups: an injection group administered three doses of spleen lymphocytes (1 × 106 , 5 × 106 , and 1 × 107 cells), a transplantation group in which a 0.25-cm2 skin section from C57BL/6 mice was transplanted onto the back of the recipient, and a control group in which an equal volume of phosphate-buffered saline was injected. At 1, 2, or 3 months following transplantation, the following parameters were evaluated: quantity of T lymphocytes, percentage of cluster of differentiation 8+ (CD8+ ) memory T cells, and proliferation index of purified CD8+ memory T cells. No significant differences among groups were detected at 1 month (p > .05). However, the injection group administered 1 × 106 cells exhibited the highest proportion of CD8+ memory T cells among all groups at 2 months, and the proportions of CD8+ T cells were higher in the three injection groups than in the skin transplantation and control groups at 3 months. The proportions of memory T cells were higher in the injection groups administered 5 × 106 or 1 × 107 cells than in the skin transplantation and control groups at 3 months. The newly established method effectively induces memory T lymphocytes via the intraperitoneal injection of spleen lymphocytes in vivo and has potential applications in the field of immunotherapy.

Keywords: CD8+ memory T cells; allogeneic skin transplantation; intraperitoneal injection.

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes* / cytology
  • CD8-Positive T-Lymphocytes* / immunology
  • Female
  • Injections, Intraperitoneal
  • Lymphocyte Transfusion
  • Lymphocytes / immunology*
  • Memory T Cells* / cytology
  • Memory T Cells* / immunology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Skin Transplantation
  • Spleen / cytology