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CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes

Author

Listed:
  • Edith M. Janssen
  • Edward E. Lemmens
  • Tom Wolfe

    (La Jolla Institute for Allergy and Immunology)

  • Urs Christen

    (La Jolla Institute for Allergy and Immunology)

  • Matthias G. von Herrath

    (La Jolla Institute for Allergy and Immunology)

  • Stephen P. Schoenberger

    (La Jolla Institute for Allergy and Immunology)

Abstract

A long-standing paradox in cellular immunology concerns the conditional requirement for CD4+ T-helper (TH) cells in the priming of cytotoxic CD8+ T lymphocyte (CTL) responses in vivo. Whereas CTL responses against certain viruses can be primed in the absence of CD4+ T cells, others, such as those mediated through ‘cross-priming’ by host antigen-presenting cells, are dependent on TH cells1,2,3,4. A clearer understanding of the contribution of TH cells to CTL development has been hampered by the fact that most TH-independent responses have been demonstrated ex vivo as primary cytotoxic effectors, whereas TH-dependent responses generally require secondary in vitro re-stimulation for their detection. Here, we have monitored the primary and secondary responses of TH-dependent and TH-independent CTLs and find in both cases that CD4+ T cells are dispensable for primary expansion of CD8+ T cells and their differentiation into cytotoxic effectors. However, secondary CTL expansion (that is, a secondary response upon re-encounter with antigen) is wholly dependent on the presence of TH cells during, but not after, priming. Our results demonstrate that T-cell help is ‘programmed’ into CD8+ T cells during priming, conferring on these cells a hallmark of immune response memory: the capacity for functional expansion on re-encounter with antigen.

Suggested Citation

  • Edith M. Janssen & Edward E. Lemmens & Tom Wolfe & Urs Christen & Matthias G. von Herrath & Stephen P. Schoenberger, 2003. "CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes," Nature, Nature, vol. 421(6925), pages 852-856, February.
  • Handle: RePEc:nat:nature:v:421:y:2003:i:6925:d:10.1038_nature01441
    DOI: 10.1038/nature01441
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    Citations

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    Cited by:

    1. Meghana Pagadala & Timothy J. Sears & Victoria H. Wu & Eva Pérez-Guijarro & Hyo Kim & Andrea Castro & James V. Talwar & Cristian Gonzalez-Colin & Steven Cao & Benjamin J. Schmiedel & Shervin Goudarzi , 2023. "Germline modifiers of the tumor immune microenvironment implicate drivers of cancer risk and immunotherapy response," Nature Communications, Nature, vol. 14(1), pages 1-22, December.
    2. Diego Calzada-Fraile & Salvador Iborra & Marta Ramírez-Huesca & Inmaculada Jorge & Enrico Dotta & Elena Hernández-García & Noa Martín-Cófreces & Estanislao Nistal-Villán & Esteban Veiga & Jesús Vázque, 2023. "Immune synapse formation promotes lipid peroxidation and MHC-I upregulation in licensed dendritic cells for efficient priming of CD8+ T cells," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    3. Joseph R. Palmeri & Brianna M. Lax & Joshua M. Peters & Lauren Duhamel & Jordan A. Stinson & Luciano Santollani & Emi A. Lutz & William Pinney & Bryan D. Bryson & K. Dane Wittrup, 2024. "CD8+ T cell priming that is required for curative intratumorally anchored anti-4-1BB immunotherapy is constrained by Tregs," Nature Communications, Nature, vol. 15(1), pages 1-19, December.
    4. Jens Bauer & Natalie Köhler & Yacine Maringer & Philip Bucher & Tatjana Bilich & Melissa Zwick & Severin Dicks & Annika Nelde & Marissa Dubbelaar & Jonas Scheid & Marcel Wacker & Jonas S. Heitmann & S, 2022. "The oncogenic fusion protein DNAJB1-PRKACA can be specifically targeted by peptide-based immunotherapy in fibrolamellar hepatocellular carcinoma," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    5. Ruka Setoguchi & Tomoya Sengiku & Hiroki Kono & Eiryo Kawakami & Masato Kubo & Tadashi Yamamoto & Shohei Hori, 2024. "Memory CD8 T cells are vulnerable to chronic IFN-γ signals but not to CD4 T cell deficiency in MHCII-deficient mice," Nature Communications, Nature, vol. 15(1), pages 1-15, December.

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