PXD066232 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Secretome of human PBMC after ConA stimulation and incubation with A1 and A2 milk fractions of different molecular weight |
| Description | There is an ongoing discussion about cow’s milk and its variants primarily focusing on the A1 variant in contrast to the A2 variant and their health-related impacts. The difference between these variants lies in a single amino acid alteration at position 67 of β-casein. This alteration is presumed to make the A1 variant more susceptible to enzymatic breakdown during milk digestion, leading to an increased release of the peptide β-casomorphin-7 (BCM-7), which is discussed to be associated with various health risks. Thus, we analyzed the influence of A1 and A2 milk on Concanavalin A (ConA)-stimulated human peripheral blood mononuclear cells (PBMCs) in earlier studies. Thereby we were able to show that milk fundamentally inhibits PBMC proliferation, independent of the β-casein variant (Gard, Flad et al. 2024). This points to an anti-proliferative effect of cow´s milk on human PBMCs, regardless of the A1 or A2 β-casein variant. In the recent study, we divided milk of both ß-casein variants in a high molecular weight (>100 kDa) and a low molecular weight (<100 kDa) protein fraction, in order to narrow down the range for the causative factor of this anti-proliferative effect triggered by the milk. The data presented here are highly relevant for human medicine and dairy industry. REFERENCE: Gard, F., L. M. Flad, T. Weisser, H. Ammer and C. A. Deeg (2024). "Effects of A1 Milk, A2 Milk and the Opioid-like Peptide beta-Casomorphin-7 on the Proliferation of Human Peripheral Blood Mononuclear Cells." Biomolecules 14(6). |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-07-13 |
| AnnouncementXML | Submission_2026-07-12_16:26:30.730.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Roxane Degroote |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; |
| ModificationList | acetylated residue; monohydroxylated residue; deamidated residue; iodoacetamide derivatized residue |
| Instrument | Q Exactive HF-X |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2025-07-16 18:58:07 | ID requested | |
| ⏵ 1 | 2026-07-12 16:26:31 | announced | |
Publication List
| Flad LM, Wei, ß, er T, Liedl J, Gard F, Petrera A, von Toerne C, Hauck SM, Deeg CA, Kleinwort KJH, Inhibitory impact of A1 and A2 cow's milk on human peripheral blood mononuclear cells identifies TOM1 as a candidate anti-inflammatory mediator. Front Immunol, 17():1728935(2026) [pubmed] |
| 10.3389/fimmu.2026.1728935; |
Keyword List
| submitter keyword: A1/A2 milk,uantitative label-free LC-MS/MS, modulation of immune system, human PBMC |
Contact List
| Stefanie M. |
| contact affiliation | Metabolomics and Proteomics Core, Helmholtz Center Munich, German Research Center for Environmental Health, D-80939 Munich, Germany |
| contact email | stefanie.hauck@helmholtz-munich.de |
| lab head | |
| Roxane Degroote |
| contact affiliation | LMU Munich, Veterinary Sciences, Chair of Physiology, Lena-Christ-Straße 48, 82152 Planegg/Martinsried, Germany |
| contact email | r.degroote@lmu.de |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/07/PXD066232 |
| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD066232
- Label: PRIDE project
- Name: Secretome of human PBMC after ConA stimulation and incubation with A1 and A2 milk fractions of different molecular weight