Development and validation of a high throughput multiplex immunofluorescence assay to detect all human immunoglobulin isotypes and subclasses in human fluids

Antibodies in human milk protect infants against infections, but currently no assay is described that is able to simultaneously measure all 9 antibody isotypes and subclasses immunoglobulins in human fluids, such as human milk. Our cohort "Protecting against Respiratory tract Infections through human Milk Analysis" (PRIMA) is focused on the relation between the occurrence of respiratory infections during the first year of life and concentration of maternal antibodies in breastfeeding. We developed and successfully validated a multiplex assay that is able to measure all nine antibody isotypes and subclasses in human plasma and milk (regardeless of the pathogen specificity), using a small sample volume. We used a multiplex immunofluorescence assay (MIA) requiring a minimal sample volume of 25 µl. Commercially available human isotype standards were used in spiking experiments to exclude the presence of cross reactivity. In addition, we prevented signal quenching by milk by determining the optimal dilution of human milk. In conclusion, we have developed a low-volume multiplex assay, that, for the first time, can reliably quantify functionally intact antibodies of all known human isotypes and subclasses and that is able to measure both kappa and lambda heavy chain antibodies. This assay can easily be implemented in other academic labs.

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Publication Details

Journal
The Journal of Immunology
Published
2025-03-06
DOI
https://doi.org/10.1093/jimmun/vkae048
Primary Topic
Respiratory viral infections research
Type
article
Field-Weighted Citation Impact
0.00

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Development and validation of a high throughput multiplex immunofluorescence assay to detect all human immunoglobulin isotypes and subclasses in human fluids

Sabine M. P. J. Prevaes, Gaby P. Smits, Jeanette H.W. Leusen, Debbie van Baarle et al.
The Journal of Immunology
Respiratory viral infections research
article

Development and validation of a high throughput multiplex immunofluorescence assay to detect all human immunoglobulin isotypes and subclasses in human fluids

Sabine M. P. J. Prevaes, Gaby P. Smits, Jeanette H.W. Leusen, Debbie van Baarle, Johan Garssen, Gerco den Hartog, Femke van Wijk, L.M.J. Knippels, Louis Bont, Laura A.P.M. Meulenbroek, Nynke Y. Rots, Martijn J. C. van Herwijnen, Rutger M. Schepp, Anneke H. Hellinga, Rob van Binnendijk, Belinda van’t Land, Marca H. M. Wauben, Pieter G. M. van Gageldonk, Maaike Nederend, Caroline G. M. de Theije, Louise Berg, Cornelis K. van der Ent, Lilly M. Verhagen, André C. Knulst, Marjan Kuijer, Kitty W.M. Bloemenkamp, Bernd Stahl, Henk J. van der Linde, Arthur H. van Stigt, Thuy-My Le
article en

Abstract

Antibodies in human milk protect infants against infections, but currently no assay is described that is able to simultaneously measure all 9 antibody isotypes and subclasses immunoglobulins in human fluids, such as human milk. Our cohort "Protecting against Respiratory tract Infections through human Milk Analysis" (PRIMA) is focused on the relation between the occurrence of respiratory infections during the first year of life and concentration of maternal antibodies in breastfeeding. We developed and successfully validated a multiplex assay that is able to measure all nine antibody isotypes and subclasses in human plasma and milk (regardeless of the pathogen specificity), using a small sample volume. We used a multiplex immunofluorescence assay (MIA) requiring a minimal sample volume of 25 µl. Commercially available human isotype standards were used in spiking experiments to exclude the presence of cross reactivity. In addition, we prevented signal quenching by milk by determining the optimal dilution of human milk. In conclusion, we have developed a low-volume multiplex assay, that, for the first time, can reliably quantify functionally intact antibodies of all known human isotypes and subclasses and that is able to measure both kappa and lambda heavy chain antibodies. This assay can easily be implemented in other academic labs.

The Journal of ImmunologyVol. 214(4)
University Medical Center Utrecht (NL), National Institute for Public Health and the Environment (NL), Danone (Netherlands) (NL), Nutricia Research (Netherlands) (NL), Wilhelmina Children's Hospital (NL), Danone Nutricia Research (Netherlands)
Danone Nutricia Research
Openalex Percentile: Top 94%
Respiratory viral infections research
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