Evidence map›Paper›PMID 32453842›Full record

ArticleBlood advances2020

Unexpected enhancement of FVIII immunogenicity by endothelial expression in lentivirus-transduced and transgenic mice.

Qizhen Shi, Christopher V Carman, Yingyu Chen, Peter T Sage, Feng Xue, Xin M Liang, Gary E Gilbert

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Application of Gene Therapy in Hemophilia.Current medical science · 2022
    Article
  6. 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 3 institutions in 1 country.

Qizhen ShiDepartment of Pediatrics, Medical College of Wisconsin, Milwaukee, WI.
Christopher V CarmanMolecular and Integrative Physiological Sciences Program, Harvard School of Public Health, Boston, MA.
Yingyu ChenDepartment of Pediatrics, Medical College of Wisconsin, Milwaukee, WI.
Peter T SageRenal Division, Transplant Research Center, Brigham and Women's Hospital and Harvard Medical School, Boston, MA; and.
Feng XueDepartment of Pediatrics, Medical College of Wisconsin, Milwaukee, WI.
Xin M LiangDepartment of Medicine, Veterans Affairs Boston Healthcare System and Harvard Medical School, Boston, MA.
Gary E GilbertDepartment of Medicine, Veterans Affairs Boston Healthcare System and Harvard Medical School, Boston, MA.
Medical College of Wisconsin · USHarvard University · USBrigham and Women's Hospital · US

Funding

Platelet-Derived FVIII Gene Therapy of Hemophilia AR01HL102035 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI Qizhen Shi · 2010 to 2026
$7.0M
Mechanisms for Maintaining Endothelial Integrity During InflammationR01HL104006 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CARMAN, CHRISTOPHER V · 2011 to 2014
$1.7M
Immune Functions of the Vascular Endothelium in Health and DiseaseR56HL111640 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CARMAN, CHRISTOPHER V · 2015 to 2015
$468k
NHLBI NIH HHS R01 HL102035NHLBI NIH HHS R01 HL104006NHLBI NIH HHS R56 HL111640
6 · The paper itself

Abstract

Factor VIII (FVIII) replacement therapy for hemophilia A is complicated by development of inhibitory antibodies (inhibitors) in ∼30% of patients. Because endothelial cells (ECs) are the primary physiologic expression site, we probed the therapeutic potential of genetically restoring FVIII expression selectively in ECs in hemophilia A mice (FVIIInull). Expression of FVIII was driven by the Tie2 promoter in the context of lentivirus (LV)-mediated in situ transduction (T2F8LV) or embryonic stem cell-mediated transgenesis (T2F8Tg). Both endothelial expression approaches were associated with a strikingly robust immune response. Following in situ T2F8LV-mediated EC transduction, all FVIIInull mice developed inhibitors but had no detectable plasma FVIII. In the transgenic approach, the T2F8Tg mice had normalized plasma FVIII levels, but showed strong sensitivity to developing an FVIII immune response upon FVIII immunization. A single injection of FVIII with incomplete Freund adjuvant led to high titers of inhibitors and reduction of plasma FVIII to undetectable levels. Because ECs are putative major histocompatibility complex class II (MHCII)-expressing nonhematopoietic, "semiprofessional" antigen-presenting cells (APCs), we asked whether they might directly influence the FVIII immune responses. Imaging and flow cytometric studies confirmed that both murine and human ECs express MHCII and efficiently bind and take up FVIII protein in vitro. Moreover, microvascular ECs preconditioned ex vivo with inflammatory cytokines could functionally present exogenously taken-up FVIII to previously primed CD4+/CXCR5+ T follicular helper (Tfh) cells to drive FVIII-specific proliferation. Our results show an unanticipated immunogenicity of EC-expressed FVIII and suggest a context-dependent role for ECs in the regulation of inhibitors as auxiliary APCs for Tfh cells.

Indexed as

Factor VIIIHemophilia AAnimalsEndothelial CellsHumansLentivirusMiceMice, TransgenicFactor VIII

Identifiers

PMID32453842
PMCPMC7252558
OpenAlexW3031995727

What OpenQuestion holds

Textmetadata
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.