Lymph node-derived donor encephalitogenic CD4+ T cells in C57BL/6 mice adoptive transfer experimental autoimmune encephalomyelitis highly express GM-CSF and T-bet
2011

Study on T Cells in Mice with Autoimmune Encephalomyelitis

publication Evidence: moderate

Author Information

Author(s): Cravens Petra D, Hussain Rehana Z, Zacharias Tresa E, Ben Li-Hong, Herndon Emily, Vinnakota Ramya, Lambracht-Washington Doris, Nessler Stefan, Zamvil Scott S, Eagar Todd N, Stüve Olaf

Primary Institution: University of Texas Southwestern Medical Center at Dallas, TX, USA

Hypothesis

The study aimed to develop a reliable protocol for inducing experimental autoimmune encephalomyelitis (EAE) in C57BL/6 mice through adoptive transfer of T cells.

Conclusion

The study successfully established a reproducible method for inducing EAE in C57BL/6 mice using donor lymph node cells that express specific inflammatory markers.

Supporting Evidence

  • Day 12 lymph node cells were able to transfer disease into recipient mice after in vitro restimulation.
  • GM-CSF levels were significantly higher in day 12 lymph node cells compared to day 6.
  • T-bet expression was maintained in the day 12 lymph node cells, which were capable of inducing EAE.

Takeaway

Researchers figured out how to make sick mice by giving them special immune cells from other mice, helping us understand diseases like multiple sclerosis better.

Methodology

The study involved immunizing donor mice with MOGp35-55 and CFA, isolating lymph node cells, and restimulating them in vitro before transferring to recipient mice.

Limitations

The study did not identify a single biomarker for encephalitogenicity, indicating a complex interplay of factors.

Participant Demographics

C57BL/6 mice were used as the primary model for the study.

Statistical Information

P-Value

p ≤ 0.001

Statistical Significance

p ≤ 0.001

Digital Object Identifier (DOI)

10.1186/1742-2094-8-73

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