Evidence map›Paper›PMID 40036068›Full record

ArticleThe Journal of clinical investigation2025

The saponin monophosphoryl lipid A nanoparticle adjuvant induces dose-dependent HIV vaccine responses in nonhuman primates.

Parham Ramezani-Rad, Ester Marina-Zárate, Laura Maiorino, Amber Myers, Katarzyna Kaczmarek Michaels, Ivan S Pires, Nathaniel I Bloom, Mariane B Melo, Ashley A Lemnios, Paul G Lopez and 18 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors.

Parham Ramezani-RadCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, California, USA.
Ester Marina-ZárateCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, California, USA.
Laura MaiorinoDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Amber MyersCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, California, USA.
Katarzyna Kaczmarek MichaelsDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Ivan S PiresDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Nathaniel I BloomCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, California, USA.
Mariane B MeloDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Ashley A LemniosDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Paul G LopezCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, California, USA.
Christopher A CottrellConsortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, USA.
Iszac BurtonConsortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, USA.
Bettina GroschelConsortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, USA.
Arpan PradhanEmory National Primate Research Center and Emory Vaccine Center, Emory University School of Medicine, Atlanta, Georgia, USA.
Gabriela StieglerPolymun Scientific Immunbiologische Forschung GmbH, Klosterneuburg, Austria.
Magdolna BudaiPolymun Scientific Immunbiologische Forschung GmbH, Klosterneuburg, Austria.
Daniel KumarPolymun Scientific Immunbiologische Forschung GmbH, Klosterneuburg, Austria.
Sam PallerlaThe International AIDS Vaccine Initiative Inc. (IAVI), New York, New York, USA.
Eddy SayeedThe International AIDS Vaccine Initiative Inc. (IAVI), New York, New York, USA.
Sangeetha L SagarThe International AIDS Vaccine Initiative Inc. (IAVI), New York, New York, USA.
Sudhir Pai KasturiEmory National Primate Research Center and Emory Vaccine Center, Emory University School of Medicine, Atlanta, Georgia, USA.
Koen Ka Van RompayCalifornia National Primate Research Center and.
Lars HangartnerConsortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, USA.
Andreas WagnerPolymun Scientific Immunbiologische Forschung GmbH, Klosterneuburg, Austria.
Dennis R BurtonConsortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, USA.
William R SchiefConsortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, USA.
Shane CrottyCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, California, USA.
Darrell J IrvineConsortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, USA.

Funding

Identification of neutralizing epitopes on SARS-CoV-2 spike for design of vaccines and small-molecule antiviralsUM1AI144462 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI BURTON, DENNIS R. · 2019 to 2025
$201.6M
National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
Nonhuman Primate Reagent ResourceU24AI126683 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Diogo Magnani · 2016 to 2026
$20.1M
Novel nanoparticulate adjuvants to enhance HIV-1 Env specific mucosal antibody responsesR01AI145640 · NIAID · EMORY UNIVERSITY · PI KASTURI, SUDHIR PAI · 2019 to 2023
$5.0M
NovaSeq5000 High Throughput SequencerS10OD025052 · OD · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SEUMOIS, GREGORY · 2018 to 2018
$832k
NIAID NIH HHS R01 AI145640NIAID NIH HHS U24 AI126683NIAID NIH HHS UM1 AI144462NIH HHS P51 OD011107NIH HHS S10 OD025052
6 · The paper itself

Abstract

Induction of durable protective immune responses is the main goal of prophylactic vaccines, and adjuvants play a role as drivers of such responses. Despite advances in vaccine strategies, development of a safe and effective HIV vaccine remains a significant challenge. Use of an appropriate adjuvant is crucial to the success of HIV vaccines. Here we assessed the saponin/MPLA nanoparticle (SMNP) adjuvant with an HIV envelope (Env) trimer, evaluating the safety and effect of multiple variables - including adjuvant dose (16-fold dose range), immunization route, and adjuvant composition - on the establishment of Env-specific memory T and B cell (TMem and BMem) responses and long-lived plasma cells in nonhuman primates (NHPs). Robust BMem were detected in all groups, but a 6-fold increase was observed in the highest- versus the lowest-SMNP-dose group. Similarly, stronger vaccine responses were induced by the highest SMNP dose in CD40L+OX40+ CD4+ TMem (11-fold), IFN-γ+ CD4+ TMem (15-fold), IL21+ CD4+ TMem (9-fold), circulating T follicular helper cells (TFH; 3.6-fold), BM plasma cells (7-fold), and binding IgG (1.3-fold). Substantial tier 2 neutralizing antibodies were only observed in the higher-SMNP-dose groups. These investigations highlight the dose-dependent potency of SMNP and its relevance for human use and next-generation vaccines.

Indexed as

Adjuvants, ImmunologicAIDS VaccinesHIV-1HIV InfectionsLipid ANanoparticlesSaponinsAnimalsB-LymphocytesFemaleHIV AntibodiesMacaca mulattaAdjuvants, ImmunologicAIDS VaccinesHIV AntibodiesLipid Amonophosphoryl lipid ASaponinsAdaptive immunityAIDS/HIVAIDS vaccineImmunology

Identifiers

PMID40036068
PMCPMC11996878

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.