Evidence map›Paper›PMID 33432229›Full record

ArticleNature immunology2021

γδ T cells suppress Plasmodium falciparum blood-stage infection by direct killing and phagocytosis.

Caroline Junqueira, Rafael B Polidoro, Guilherme Castro, Sabrina Absalon, Zhitao Liang, Sumit Sen Santara, Ângela Crespo, Dhelio B Pereira, Ricardo T Gazzinelli, Jeffrey D Dvorin and 1 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Nature immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
12.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 84 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Cell stress activates γ9δ2 T cells via endogenous phosphoantigens and butyrophilin complex dynamics.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Impact ofTropical medicine and infectious disease · 2025
    Article
  14. CXCR6bioRxiv : the preprint server for biology · 2025
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 2 countries.

Caroline Junqueira *Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, USA. caroline.junqueira@fiocruz.br.ORCID http://orcid.org/0000-0003-0545-0986
Rafael B Polidoro *Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, USA.
Guilherme CastroInstituto René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, MG, Brazil.
Sabrina AbsalonDepartment of Pediatrics, Harvard Medical School, Boston, MA, USA.
Zhitao LiangProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0001-5320-6107
Sumit Sen SantaraProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, USA.
Ângela CrespoProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, USA.
Dhelio B PereiraCentro de Pesquisa em Medicina Tropical de Rondônia, Porto Velho, RO, Brazil.ORCID http://orcid.org/0000-0002-7761-5498
Ricardo T GazzinelliInstituto René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, MG, Brazil.
Jeffrey D DvorinDepartment of Pediatrics, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-5883-7271
Judy LiebermanProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, USA. judy.lieberman@childrens.harvard.edu.ORCID http://orcid.org/0000-0002-6200-4715
Boston Children's Hospital · USUniversidade Federal de Minas Gerais · BR

Funding

Sugar-feeding behavior of the malaria vector Nyssorhynchus darlingi and development of effective attractive toxic sugar baits (ATSB) to increase intervention success in PeruU19AI089681 · NIAID · YALE UNIVERSITY · PI CASTRO, MARCIA C. · 2010 to 2023
$20.1M
Granzyme and Granulysin Mediated Death of Trypanosoma cruziR01AI116577 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI GAZZINELLI, RICARDO TOSTES, LIEBERMAN, JUDY · 2016 to 2020
$3.2M
Molecular mechanisms of schizogony in malaria parasitesR01AI145941 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI DVORIN, JEFFREY D · 2019 to 2023
$3.1M
Monocyte-derived dendritic cells in malariaR01NS098747 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GAZZINELLI, RICARDO TOSTES, LUSTER, ANDREW D · 2016 to 2020
$2.1M
Killing of P. vivax infected reticulocytes by cytotoxic T cellsR21AI131632 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GAZZINELLI, RICARDO TOSTES, LIEBERMAN, JUDY · 2018 to 2019
$484k
Host Ciracadian Clock and MalariaR21AI150546 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GAZZINELLI, RICARDO TOSTES · 2020 to 2021
$461k
NIAID NIH HHS R01 AI116577NIAID NIH HHS R01 AI145941NIAID NIH HHS R21 AI131632NIAID NIH HHS R21 AI150546NIAID NIH HHS U19 AI089681NINDS NIH HHS R01 NS098747
6 · The paper itself

Abstract

Activated Vγ9Vδ2 (γδ2) T lymphocytes that sense parasite-produced phosphoantigens are expanded in Plasmodium falciparum-infected patients. Although previous studies suggested that γδ2 T cells help control erythrocytic malaria, whether γδ2 T cells recognize infected red blood cells (iRBCs) was uncertain. Here we show that iRBCs stained for the phosphoantigen sensor butyrophilin 3A1 (BTN3A1). γδ2 T cells formed immune synapses and lysed iRBCs in a contact, phosphoantigen, BTN3A1 and degranulation-dependent manner, killing intracellular parasites. Granulysin released into the synapse lysed iRBCs and delivered death-inducing granzymes to the parasite. All intra-erythrocytic parasites were susceptible, but schizonts were most sensitive. A second protective γδ2 T cell mechanism was identified. In the presence of patient serum, γδ2 T cells phagocytosed and degraded opsonized iRBCs in a CD16-dependent manner, decreasing parasite multiplication. Thus, γδ2 T cells have two ways to control blood-stage malaria-γδ T cell antigen receptor (TCR)-mediated degranulation and phagocytosis of antibody-coated iRBCs.

Indexed as

Cytotoxicity, ImmunologicLymphocyte ActivationPhagocytosisAntigens, CDAntigens, Differentiation, T-LymphocyteAntigens, ProtozoanBostonBrazilButyrophilinsCells, CulturedErythrocytesFemaleGranzymesHost-Parasite InteractionsHumansImmunological SynapsesAntigens, CDAntigens, Differentiation, T-LymphocyteAntigens, ProtozoanBTN2A1 protein, humanBTN3A1 protein, humanButyrophilinsGNLY protein, humanGranzymesGZMB protein, human

Identifiers

PMID33432229
PMCPMC7906917
OpenAlexW3121056531

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.