Evidence map›Paper›PMID 26307241›Full record

ArticleClinical and experimental immunology2016

Anti-CD20 monoclonal antibody-dependent phagocytosis of chronic lymphocytic leukaemia cells by autologous macrophages.

A K Church, K R VanDerMeid, N A Baig, A M Baran, T E Witzig, G S Nowakowski, C S Zent

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Clinical and experimental immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.2field-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

29 citing papers in PubMed, 48 citations in OpenAlex.

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  20. Complement System: a Neglected Pathway in Immunotherapy.Clinical reviews in allergy & immunology · 2020
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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 2 institutions in 1 country.

A K ChurchDivision of Hematology, Mayo Clinic, Rochester, MN.
K R VanDerMeidWilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, USA.
N A BaigDivision of Hematology, Mayo Clinic, Rochester, MN.
A M BaranWilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, USA.
T E WitzigDivision of Hematology, Mayo Clinic, Rochester, MN.
G S NowakowskiDivision of Hematology, Mayo Clinic, Rochester, MN.
C S ZentWilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, USA.
Mayo Clinic in Arizona · USUniversity of Rochester Medical Center · US

Funding

The Role of Monocytes in non-Hodgkin LymphomaP50CA097274 · NCI · UNIVERSITY OF IOWA · PI WEINER, GEORGE J. · 2002 to 2021
$45.7M
NCI NIH HHS CA097274NCI NIH HHS P50 CA097274
6 · The paper itself

Abstract

Unconjugated monoclonal antibodies (mAbs) are an important component of effective combination therapies for chronic lymphocytic leukaemia (CLL). Antibody-dependent phagocytosis (ADP) is a major mediator of mAb cytotoxicity, but there is limited knowledge of the determinants of ADP efficacy. We used macrophages derived in vitro from autologous circulating monocytes to test the effects of mAb structure and concentration, target : effector cell ratio, duration of co-incubation and CLL cell CD20 expression on ADP. Next-generation anti-CD20 mAbs (ofatumumab, ublituximab, obinutuzumab, ocaratuzumab) were significantly more effective at inducing ADP compared to rituximab, but none were as effective as the anti-CD52 mAb alemtuzumab. Ofatumumab (10 μg/ml) used as a representative next-generation anti-CD20 mAb achieved an ADP plateau at 3 h co-incubation with a target : effector ratio of 10 : 1 (mean = 2.1 CLL cells/macrophage, range = 1.5-3.5). At 0.156 μg/ml (the lowest concentration tested) ofatumumab ADP was significantly higher than alemtuzumab. However, ofatumumab-induced ADP did not increase significantly at higher mAb concentrations. We show that anti-CD20 mAb ADP efficacy is determined by the mAb characteristics, target : effector ratio and incubation time. We suggest that preclinical evaluation of anti-CD20 mAbs to understand the determinants of ADP could be useful in designing future combination therapies for CLL.

Indexed as

AlemtuzumabAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedCell DifferentiationCells, CulturedDrug Therapy, CombinationHumansImmunotherapyLeukemia, Lymphocytic, Chronic, B-CellMacrophagesPhagocytosisRituximabAlemtuzumabAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedofatumumabRituximabalemtuzumabantibody-dependent phagocytosisanti-CD20 monoclonal antibodieschronic lymphocytic leukaemiaCLLmacrophageobinotuzumabocaratuzumabofatumumabrituximabublituximab

Identifiers

PMID26307241
PMCPMC4687519
OpenAlexW2152652891

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.