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Acute Neonatal Infections ‘Lock-In’ a Suboptimal CD8+ T Cell Repertoire with Impaired Recall Responses


Microbial infection during various stages of human development produces widely different clinical outcomes, yet the links between age-related changes in the immune compartment and functional immunity remain unclear. The ability of the immune system to respond to specific antigens and mediate protection in early life is closely correlated with the level of diversification of lymphocyte antigen receptors. We have previously shown that the neonatal primary CD8+ T cell response to replication competent virus is significantly constricted compared to the adult response. In the present study, we have analyzed the subsequent formation of neonatal memory CD8+ T cells and their response to secondary infectious challenge. In particular, we asked whether the less diverse CD8+ T cell clonotypes that are elicited by neonatal vaccination with replication competent virus are ‘locked-in’ to the adult memory T cell, and thus may compromise the strength of adult immunity. Here we report that neonatal memory CD8+ T cells mediate poor recall responses compared to adults and are comprised of a repertoire of lower avidity T cells. During a later infectious challenge the neonatal memory CD8+ T cells compete poorly with the fully diverse repertoire of naïve adult CD8+ T cells and are outgrown by the adult primary response. This has important implications for the timing of vaccination in early life.


Vyšlo v časopise: Acute Neonatal Infections ‘Lock-In’ a Suboptimal CD8+ T Cell Repertoire with Impaired Recall Responses. PLoS Pathog 9(9): e32767. doi:10.1371/journal.ppat.1003572
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1003572

Souhrn

Microbial infection during various stages of human development produces widely different clinical outcomes, yet the links between age-related changes in the immune compartment and functional immunity remain unclear. The ability of the immune system to respond to specific antigens and mediate protection in early life is closely correlated with the level of diversification of lymphocyte antigen receptors. We have previously shown that the neonatal primary CD8+ T cell response to replication competent virus is significantly constricted compared to the adult response. In the present study, we have analyzed the subsequent formation of neonatal memory CD8+ T cells and their response to secondary infectious challenge. In particular, we asked whether the less diverse CD8+ T cell clonotypes that are elicited by neonatal vaccination with replication competent virus are ‘locked-in’ to the adult memory T cell, and thus may compromise the strength of adult immunity. Here we report that neonatal memory CD8+ T cells mediate poor recall responses compared to adults and are comprised of a repertoire of lower avidity T cells. During a later infectious challenge the neonatal memory CD8+ T cells compete poorly with the fully diverse repertoire of naïve adult CD8+ T cells and are outgrown by the adult primary response. This has important implications for the timing of vaccination in early life.


Zdroje

1. AdkinsB, LeclercC, Marshall-ClarkeS (2004) Neonatal adaptive immunity comes of age. Nat Rev Immunol 4: 553–564.

2. SiegristCA (2001) Neonatal and early life vaccinology. Vaccine 19: 3331–3346.

3. WilsonCB, KollmannTR (2008) Induction of antigen-specific immunity in human neonates and infants. Nestle Nutr Workshop Ser Pediatr Program 61: 183–195.

4. Nikolich-ZugichJ, FremontDH, MileyMJ, MessaoudiI (2004) The role of mhc polymorphism in anti-microbial resistance. Microbes Infect 6: 501–512.

5. Nikolich-ZugichJ, SlifkaMK, MessaoudiI (2004) The many important facets of T-cell repertoire diversity. Nat Rev Immunol 4: 123–132.

6. DavisMM, BjorkmanPJ (1988) T-cell antigen receptor genes and T-cell recognition. Nature 334: 395–402.

7. LandrethKS, McCoyK, ClagettJ, BollumFJ, RosseC (1981) Deficiency in cells expressing terminal transferase in autoimmune (motheaten) mice. Nature 290: 409–411.

8. CabaniolsJP, FazilleauN, CasrougeA, KourilskyP, KanellopoulosJM (2001) Most alpha/beta T cell receptor diversity is due to terminal deoxynucleotidyl transferase. J Exp Med 194: 1385–1390.

9. FeeneyAJ (1991) Junctional sequences of fetal T cell receptor beta chains have few N regions. J Exp Med 174: 115–124.

10. BogueM, CandeiasS, BenoistC, MathisD (1991) A special repertoire of alpha:beta T cells in neonatal mice. Embo J 10: 3647–3654.

11. RuddBD, VenturiV, DavenportMP, Nikolich-ZugichJ (2011) Evolution of the antigen-specific CD8+ TCR repertoire across the life span: evidence for clonal homogenization of the old TCR repertoire. J Immunol 186: 2056–2064.

12. RuddBD, VenturiV, SmitheyMJ, WaySS, DavenportMP, et al. (2010) Diversity of the CD8+ T cell repertoire elicited against an immunodominant epitope does not depend on the context of infection. J Immunol 184: 2958–2965.

13. WallaceME, KeatingR, HeathWR, CarboneFR (1999) The cytotoxic T-cell response to herpes simplex virus type 1 infection of C57BL/6 mice is almost entirely directed against a single immunodominant determinant. J Virol 73: 7619–7626.

14. RidgeJP, FuchsEJ, MatzingerP (1996) Neonatal tolerance revisited: turning on newborn T cells with dendritic cells. Science 271: 1723–1726.

15. GarciaAM, FadelSA, CaoS, SarzottiM (2000) T cell immunity in neonates. Immunol Res 22: 177–190.

16. RuddBD, VenturiV, SmitheyMJ, WaySS, DavenportMP, et al. (2010) Diversity of the CD8+ T cell repertoire elicited against an immunodominant epitope does not depend on the context of infection. Journal of immunology 184: 2958–2965.

17. MessaoudiI, Guevara PatinoJA, DyallR, LeMaoultJ, Nikolich-ZugichJ (2002) Direct link between mhc polymorphism, T cell avidity, and diversity in immune defense. Science 298: 1797–1800.

18. HaleJS, BoursalianTE, TurkGL, FinkPJ (2006) Thymic output in aged mice. Proc Natl Acad Sci U S A 103: 8447–8452.

19. HaeryfarSM, HickmanHD, IrvineKR, TscharkeDC, BenninkJR, et al. (2008) Terminal deoxynucleotidyl transferase establishes and broadens antiviral CD8+ T cell immunodominance hierarchies. J Immunol 181: 649–659.

20. KedzierskaK, ThomasPG, VenturiV, DavenportMP, DohertyPC, et al. (2008) Terminal deoxynucleotidyltransferase is required for the establishment of private virus-specific CD8+ TCR repertoires and facilitates optimal CTL responses. J Immunol 181: 2556–2562.

21. RuckwardtTJ, MalloyAM, GostickE, PriceDA, DashP, et al. (2011) Neonatal CD8 T-cell hierarchy is distinct from adults and is influenced by intrinsic T cell properties in respiratory syncytial virus infected mice. PLoS pathogens 7: e1002377.

22. CasrougeA, BeaudoingE, DalleS, PannetierC, KanellopoulosJ, et al. (2000) Size estimate of the alpha beta TCR repertoire of naive mouse splenocytes. J Immunol 164: 5782–5787.

23. MaryanskiJL, JongeneelCV, BucherP, CasanovaJL, WalkerPR (1996) Single-cell PCR analysis of TCR repertoires selected by antigen in vivo: a high magnitude CD8 response is comprised of very few clones. Immunity 4: 47–55.

24. KellyKA, ScollayR (1992) Seeding of neonatal lymph nodes by T cells and identification of a novel population of CD3-CD4+ cells. Eur J Immunol 22: 329–334.

25. Le CampionA, BourgeoisC, LambolezF, MartinB, LeaumentS, et al. (2002) Naive T cells proliferate strongly in neonatal mice in response to self-peptide/self-MHC complexes. Proc Natl Acad Sci U S A 99: 4538–4543.

26. PriceDA, WestSM, BettsMR, RuffLE, BrenchleyJM, et al. (2004) T cell receptor recognition motifs govern immune escape patterns in acute SIV infection. Immunity 21: 793–803.

27. Meyer-OlsonD, ShoukryNH, BradyKW, KimH, OlsonDP, et al. (2004) Limited T cell receptor diversity of HCV-specific T cell responses is associated with CTL escape. The Journal of experimental medicine 200: 307–319.

28. CornbergM, ChenAT, WilkinsonLA, BrehmMA, KimSK, et al. (2006) Narrowed TCR repertoire and viral escape as a consequence of heterologous immunity. The Journal of clinical investigation 116: 1443–1456.

29. PriceDA, AsherTE, WilsonNA, NasonMC, BrenchleyJM, et al. (2009) Public clonotype usage identifies protective Gag-specific CD8+ T cell responses in SIV infection. The Journal of experimental medicine 206: 923–936.

30. HaluszczakC, AkueAD, HamiltonSE, JohnsonLD, PujanauskiL, et al. (2009) The antigen-specific CD8+ T cell repertoire in unimmunized mice includes memory phenotype cells bearing markers of homeostatic expansion. The Journal of experimental medicine 206: 435–448.

31. HoltappelsR, JandaJ, ThomasD, SchenkS, ReddehaseMJ, et al. (2008) Adoptive CD8 T cell control of pathogens cannot be improved by combining protective epitope specificities. The Journal of infectious diseases 197: 622–629.

32. HamiltonSE, JamesonSC (2012) CD8 T cell memory: it takes all kinds. Front Immunol 3: 353.

33. LangA, BrienJD, MessaoudiI, Nikolich-ZugichJ (2008) Age-related dysregulation of CD8+ T cell memory specific for a persistent virus is independent of viral replication. J Immunol 180: 4848–4857.

34. LangA, Nikolich-ZugichJ (2005) Development and migration of protective CD8+ T cells into the nervous system following ocular herpes simplex virus-1 infection. J Immunol 174: 2919–2925.

35. RuddBD, VenturiV, LiG, SamadderP, ErteltJM, et al. (2011) Nonrandom attrition of the naive CD8+ T-cell pool with aging governed by T-cell receptor:pMHC interactions. Proceedings of the National Academy of Sciences of the United States of America 108: 13694–13699.

36. LefrancMP, GiudicelliV, GinestouxC, BodmerJ, MullerW, et al. (1999) IMGT, the international ImMunoGeneTics database. Nucleic Acids Res 27: 209–212.

37. VenturiV, KedzierskaK, TurnerSJ, DohertyPC, DavenportMP (2007) Methods for comparing the diversity of samples of the T cell receptor repertoire. Journal of Immunological Methods 321: 182–195.

38. OrrMT, OrgunNN, WilsonCB, WaySS (2007) Cutting Edge: Recombinant Listeria monocytogenes expressing a single immune-dominant peptide confers protective immunity to herpes simplex virus-1 infection. J Immunol 178: 4731–4735.

39. ChothiaC, BoswellDR, LeskAM (1988) The outline structure of the T-cell alpha beta receptor. Embo J 7: 3745–3755.

Štítky
Hygiena a epidemiológia Infekčné lekárstvo Laboratórium

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