Evidence map›Paper›PMID 42821149›Full record

ArticleAMB Express2026

A novel synergistic phycobiliprotein combination against HIV-1 shows potent antiviral activity.

Pratiksha Jadaun, R Harshithkumar, Ishrat Khan, Debashree Dass, Pooja Wakchaure, Ruchi Kadam, Ashwini More, Kishore Dhotre, Nikhat J Siddiqi, Ahmed Alsadoun and 5 more

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Article in AMB Express, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Pratiksha Jadaun *ICMR-National Institute of Translational Virology and AIDS Research, 73G, MIDC Bhosari, Pune, India. paj.sbas@jspmuni.ac.in.
R Harshithkumar *ICMR-National Institute of Translational Virology and AIDS Research, 73G, MIDC Bhosari, Pune, India.
Ishrat KhanICMR-National Institute of Translational Virology and AIDS Research, 73G, MIDC Bhosari, Pune, India.
Debashree DassICMR-National Institute of Translational Virology and AIDS Research, 73G, MIDC Bhosari, Pune, India.
Pooja WakchaureICMR-National Institute of Translational Virology and AIDS Research, 73G, MIDC Bhosari, Pune, India.
Ruchi KadamICMR-National Institute of Translational Virology and AIDS Research, 73G, MIDC Bhosari, Pune, India.
Ashwini MoreICMR-National Institute of Translational Virology and AIDS Research, 73G, MIDC Bhosari, Pune, India.
Kishore DhotreInstitute for Clinical and Molecular Virology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
Nikhat J SiddiqiDepartment of Medical Surgical Nursing, College of Nursing, King Saud University, Riyadh, Saudi Arabia.
Ahmed AlsadounDepartment of Medical Surgical Nursing, College of Nursing, King Saud University, Riyadh, Saudi Arabia.
Abdul MalikDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Shyam Sundar NandiICMR-National Institute of Virology, 20A, Dr. Ambedkar Road, Pune, India.
Vijay NemaICMR-National Institute of Translational Virology and AIDS Research, 73G, MIDC Bhosari, Pune, India.
Abdul Arif KhanICMR-National Institute of Translational Virology and AIDS Research, 73G, MIDC Bhosari, Pune, India.
Anupam MukherjeeICMR-National Institute of Translational Virology and AIDS Research, 73G, MIDC Bhosari, Pune, India. mukherjee.a@icmr.gov.in.ORCID https://orcid.org/0000-0002-0612-2258

Funding

Department of Health Research (DHR) Women Scientist Grant WSS/2020/000023/AP_WSSKing Saud University ORF-2026-1115
6 · The paper itself

Abstract

Human immunodeficiency virus type 1 (HIV-1) remains a major global public health challenge due to lifelong persistence, latency, and the emergence of drug resistance. Natural bioactive compounds are increasingly being explored as alternative or adjunct antiviral strategies. In this study, we evaluated the antiviral efficacy and cytotoxicity of a synergistic pharmaceutical composition comprising three phycobiliproteins: C-phycocyanin (C-PC), B-phycoerythrin (B-PE), and allophycocyanin (APC), derived from cyanobacteria and marine algae. Individual and combinatorial effects were assessed against HIV-1 using TZM-bl cells and peripheral blood mononuclear cells (PBMCs). A Box-Behnken experimental design was employed to identify optimal synergistic ratios. Among fifteen combinations initially screened at a fixed concentration of 50 µg/mL, five exhibited strong antiviral activity. The optimized formulation (CBA: C2; 73.28% C-PC, 20.70% B-PE, and 6.02% APC) produced up to ~ 100% inhibition of HIV-1 during the screening assay. Subsequent dose-response analyses demonstrated IC

Indexed as

AllophycocyaninBox–Behnken designB-PhycoerythrinC-PhycocyaninHIV-1Marine bioactivesMulti-target enzyme inhibitionNatural antiviralsPhycobiliproteinsSynergistic antiviral therapy

Identifiers

What Socratic holds

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Registered trials

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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.