Evidence map›Paper›PMID 24478094›Full record

ArticleInfection and immunity2014

Model for in vivo assessment of humoral protection against malaria sporozoite challenge by passive transfer of monoclonal antibodies and immune serum.

Brandon K Sack, Jessica L Miller, Ashley M Vaughan, Alyse Douglass, Alexis Kaushansky, Sebastian Mikolajczak, Alida Coppi, Gloria Gonzalez-Aseguinolaza, Moriya Tsuji, Fidel Zavala and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
9.1field-weighted citation impact, top 2% 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

55 citing papers in PubMed, 92 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Protection from malaria infection using liver-targeted siRNA.Molecular therapy. Methods & clinical development · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Monoclonal antibodies for malaria prevention.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Review
  14. Host-parasite interactions duringFrontiers in immunology · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  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

12 authors at 6 institutions in 2 countries.

Brandon K SackSeattle Biomedical Research Institute, Seattle, Washington, USA.
Jessica L Miller
Ashley M Vaughan
Alyse Douglass
Alexis Kaushansky
Sebastian Mikolajczak
Alida Coppi
Gloria Gonzalez-Aseguinolaza
Moriya Tsuji
Fidel Zavala
Photini Sinnis
Stefan H I Kappe
Center for Infectious Disease Research · USJohns Hopkins University · USRegeneron (United States) · USRockefeller University · USUniversidad de Navarra · ESUniversity of Washington · US

Funding

EFFECTOR AND MEMORY ANTIMALARIA CD8+ CELL RESPONSESR01AI044375 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ZAVALA, FIDEL P · 1999 to 2013
$6.5M
Structure and Function of the Circumsporozoite ProteinR01AI056840 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SINNIS, PHOTINI · 2005 to 2014
$3.8M
T cell immunity to Plasmodium sporozoite immunizationR01AI095178 · NIAID · UNIVERSITY OF IOWA · PI HARTY, JOHN T · 2012 to 2016
$2.6M
NIAID NIH HHS R01 AI044375NIAID NIH HHS R01 AI056840NIAID NIH HHS R01 AI095178NIAID NIH HHS R01AI095178
6 · The paper itself

Abstract

Evidence from clinical trials of malaria vaccine candidates suggests that both cell-mediated and humoral immunity to pre-erythrocytic parasite stages can provide protection against infection. Novel pre-erythrocytic antibody (Ab) targets could be key to improving vaccine formulations, which are currently based on targeting antigens such as the circumsporozoite protein (CSP). However, methods to assess the effects of sporozoite-specific Abs on pre-erythrocytic infection in vivo remain underdeveloped. Here, we combined passive transfer of monoclonal Abs (MAbs) or immune serum with a luciferase-expressing Plasmodium yoelii sporozoite challenge to assess Ab-mediated inhibition of liver infection in mice. Passive transfer of a P. yoelii CSP MAb showed inhibition of liver infection when mice were challenged with sporozoites either intravenously or by infectious mosquito bite. However, inhibition was most potent for the mosquito bite challenge, leading to a more significant reduction of liver-stage burden and even a lack of progression to blood-stage parasitemia. This suggests that Abs provide effective protection against a natural infection. Inhibition of liver infection was also achieved by passive transfer of immune serum from whole-parasite-immunized mice. Furthermore, we demonstrated that passive transfer of a MAb against P. falciparum CSP inhibited liver-stage infection in a humanized mouse/P. falciparum challenge model. Together, these models constitute unique and sensitive in vivo methods to assess serum-transferable protection against Plasmodium sporozoite challenge.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, ProtozoanDisease Models, AnimalFemaleHumansImmune SeraImmunization, PassiveLiverMalariaMiceMice, Inbred BALB CMice, SCIDPlasmodium falciparumPlasmodium yoeliiAntibodies, MonoclonalAntibodies, ProtozoanImmune Sera

Identifiers

PMID24478094
PMCPMC3911395
OpenAlexW2133680599

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.