Evidence map›Paper›PMID 35931612›Full record

ReviewTrends in immunology2022

High endothelial venules as potential gateways for therapeutics.

Bilal Hussain, Vivek Kasinath, Gabriel P Ashton-Rickardt, Thomas Clancy, Kenji Uchimura, George Tsokos, Reza Abdi

Open access · bronzeAbstract readReview
In one paragraph

Review in Trends in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Bilal HussainTransplantation Research Center and Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Vivek KasinathTransplantation Research Center and Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Gabriel P Ashton-RickardtBrandeis University, Waltham, MA, USA.
Thomas ClancyDivision of Surgical Oncology, Brigham and Women's Hospital, Boston, MA, USA.
Kenji UchimuraUniversity Lille, CNRS, UMR8576 - UGSF - Unite de Glycogiologie Structurale et Functionelle, 59000 Lille, France.
George TsokosDivision of Rheumatology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Reza AbdiTransplantation Research Center and Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA. Electronic address: rabdi@rics.bwh.harvard.edu.
Brigham and Women's Hospital · USBeth Israel Deaconess Medical Center · USBrandeis University · USCentre National de la Recherche Scientifique · FR

Funding

Reshaping lymph node stroma for transplant toleranceP01AI153003 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Jonathan S Bromberg · 2020 to 2026
$9.3M
A novel approach to delivering therapeutics in heart transplantationR01HL145813 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ABDI, REZA · 2019 to 2022
$2.6M
IRI, innate immunity and transplant rejectionR01AI156084 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI ABDI, REZA · 2021 to 2025
$2.3M
Role of Kidney-Draining Lymph Node in Crescentic GlomerulonephritisK08DK124685 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI KASINATH, VIVEK · 2020 to 2024
$844k
NHLBI NIH HHS R01 HL145813NIAID NIH HHS P01 AI153003NIAID NIH HHS R01 AI156084NIDDK NIH HHS K08 DK124685
6 · The paper itself

Abstract

High endothelial venules (HEVs) are specialized blood vessels that support the migration of lymphocytes from the bloodstream into lymph nodes (LNs). They are also formed ectopically in mammalian organs affected by chronic inflammation and cancer. The recent arrival of immunotherapy at the forefront of many cancer treatment regimens could boost a crucial role for HEVs as gateways for the treatment of cancer. In this review, we describe the microanatomical and biochemical characteristics of HEVs, mechanisms of formation of newly made HEVs, immunotherapies potentially dependent on HEV-mediated T cell homing to tumors, and finally, how HEV-targeted therapies might be used as a complementary approach to potentially shape the therapeutic landscape for the treatment of cancer and immune-mediated diseases.

Indexed as

Lymph NodesNeoplasmsAnimalsHumansLymphocytesMammalsT-LymphocytesVenulescancer immunologyhigh endothelial venulelymph nodenanomedicinenanoparticlestransplantation

Identifiers

PMID35931612
PMCPMC10804419
OpenAlexW4289527297

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.