Cd4+ t cell transplantation

Cd4+ t cell transplantation has been studied in 1 paper since 2021: none in people yet, 1 in animals. The research so far is in animals. The newest paper, Feb 19, 2021: “Terminally Differentiated CD4⁺ T Cells Promote Myocardial Inflammaging”.

Intervention

1 paper studies it3 findingsUpdated

See all 1 papers on cd4+ t cell transplantation

At a glance

The findings reach mice, none yet in people. 1 lab in 1 country.

None of its findings points the other way.

Mice: a single group. Cells, worms or flies and humans: nothing yet.
  • 1 lab in 1 country
  • Funders: Agence Nationale de la Recherche and 4 more
  • Animals1

What did studies of cd4+ t cell transplantation find?

3

Studies of cd4+ t cell transplantation measured 3 outcomes; the most studied are inflammation (1 study), myocardial immune cell infiltration (1) and CD4+ T cell terminal differentiation (1).

Inflammation

upin mice1

1 study
  1. Cd4+ t cell transplantation increases inflammation in young NSG-DR1 mice.

    “expanding T-cells promote myocardial inflammaging, marked by a distinct age-related transcriptomic signature”

    Animalsin young NSG-DR1 micemyocardium

    Terminally Differentiated CD4⁺ T Cells Promote Myocardial Inflammaging

    Frontiers in immunology

More on Inflammation

Myocardial immune cell infiltration

upin mice1

1 study
  1. Cd4+ t cell transplantation increases myocardial immune cell infiltration in young NSG-DR1 mice.

    “young mice harboring an expanded CD4+ T cell compartment showed increased numbers of infiltrating monocytes, macrophages and dendritic cells in the heart”

    Animalsin young NSG-DR1 miceheart

    Terminally Differentiated CD4⁺ T Cells Promote Myocardial Inflammaging

    Frontiers in immunology

CD4+ T cell terminal differentiation

upin mice1

1 study
  1. Cd4+ t cell transplantation induces CD4+ T cell terminal differentiation in young lymphocyte-deficient NSG-DR1 mice.

    “CD4+ T cells underwent homeostatic expansion, upregulated expression of PD-1 receptor and strongly shifted towards effector/memory (CCR7− CD45RO+) and terminally-differentiated phenotypes (CCR7−CD45RO−)”

    Animalsin young lymphocyte-deficient NSG-DR1 mice

    Terminally Differentiated CD4⁺ T Cells Promote Myocardial Inflammaging

    Frontiers in immunology

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