Free light chains as an emerging biomarker in saliva: Biological variability and comparisons with salivary IgA and steroid hormones.


Journal

Brain, behavior, and immunity
ISSN: 1090-2139
Titre abrégé: Brain Behav Immun
Pays: Netherlands
ID NLM: 8800478

Informations de publication

Date de publication:
01 2020
Historique:
received: 16 07 2019
revised: 10 09 2019
accepted: 23 09 2019
pubmed: 27 9 2019
medline: 9 3 2021
entrez: 27 9 2019
Statut: ppublish

Résumé

Salivary free light chains (FLCs) are an emerging biomarker in health and behavioural research. However, little is known regarding biological variability of salivary FLCs and how they relate to other established salivary biomarkers. This study aimed to investigate the diurnal and day-to-day variation of salivary FLCs and their relationship with salivary IgA and steroid hormones. A total of 46 healthy adults participated in studies exploring the biological variability of FLCs. Diurnal variation was investigated by collecting saliva samples immediately upon waking, 0.5 h, 3 h, 6 h, 9 h and 14 h post-waking. Saliva samples were assessed for FLCs, IgA, cortisol and dehydroepiandrosterone (DHEA). Between-day variation in FLCs and IgA was assessed by collecting saliva samples immediately upon waking for seven consecutive days. Participants underwent a dental examination to exclude oral health as a potential confounding variable. Within and between-person day-to day variation was explored in relation to a range of different factors: awakening time, sleep, exercise, well-being and alcohol consumption. Salivary secretion rates of FLCs decreased following waking and up to 3 h post-waking and then plateaued. This same pattern was observed for IgA. DHEA was stable upon waking and higher levels were seen in the morning with significantly lower levels thereafter. Cortisol levels significantly increased 0.5 h post-waking then continued to decline across the day. FLCs were significantly correlated with IgA but not cortisol or DHEA. Both FLCs and IgA parameters showed day-to-day variability, with coefficients of variation ≥ 40%. Earlier waking time was significantly correlated with higher FLC and IgA secretion rates. Inter-person differences in saliva parameter variability were observed but the degree of variation in FLCs and IgA was related within person. Inter-person day-to-day variation appeared to be uninfluenced by lifestyle or behavioural factors. Saliva FLCs secretion exhibits diurnal fluctuation that mirrors IgA fluctuation. Findings strongly indicate salivary FLC secretion is orchestrated by local plasma cells. FLCs and IgA both showed notable variability day-to-day, which was similar within person and influenced by awakening time. FLCs offer a promising adjunct to IgA in the measurement of oral immune activation.

Sections du résumé

BACKGROUND
Salivary free light chains (FLCs) are an emerging biomarker in health and behavioural research. However, little is known regarding biological variability of salivary FLCs and how they relate to other established salivary biomarkers. This study aimed to investigate the diurnal and day-to-day variation of salivary FLCs and their relationship with salivary IgA and steroid hormones.
METHODS
A total of 46 healthy adults participated in studies exploring the biological variability of FLCs. Diurnal variation was investigated by collecting saliva samples immediately upon waking, 0.5 h, 3 h, 6 h, 9 h and 14 h post-waking. Saliva samples were assessed for FLCs, IgA, cortisol and dehydroepiandrosterone (DHEA). Between-day variation in FLCs and IgA was assessed by collecting saliva samples immediately upon waking for seven consecutive days. Participants underwent a dental examination to exclude oral health as a potential confounding variable. Within and between-person day-to day variation was explored in relation to a range of different factors: awakening time, sleep, exercise, well-being and alcohol consumption.
RESULTS
Salivary secretion rates of FLCs decreased following waking and up to 3 h post-waking and then plateaued. This same pattern was observed for IgA. DHEA was stable upon waking and higher levels were seen in the morning with significantly lower levels thereafter. Cortisol levels significantly increased 0.5 h post-waking then continued to decline across the day. FLCs were significantly correlated with IgA but not cortisol or DHEA. Both FLCs and IgA parameters showed day-to-day variability, with coefficients of variation ≥ 40%. Earlier waking time was significantly correlated with higher FLC and IgA secretion rates. Inter-person differences in saliva parameter variability were observed but the degree of variation in FLCs and IgA was related within person. Inter-person day-to-day variation appeared to be uninfluenced by lifestyle or behavioural factors.
CONCLUSIONS
Saliva FLCs secretion exhibits diurnal fluctuation that mirrors IgA fluctuation. Findings strongly indicate salivary FLC secretion is orchestrated by local plasma cells. FLCs and IgA both showed notable variability day-to-day, which was similar within person and influenced by awakening time. FLCs offer a promising adjunct to IgA in the measurement of oral immune activation.

Identifiants

pubmed: 31557507
pii: S0889-1591(19)30763-9
doi: 10.1016/j.bbi.2019.09.018
pii:
doi:

Substances chimiques

Biomarkers 0
Immunoglobulin A 0
Dehydroepiandrosterone 459AG36T1B
Hydrocortisone WI4X0X7BPJ

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

78-86

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Alec Rapson (A)

Institute of Immunology and Immunotherapy, University of Birmingham, UK.

Emily Collman (E)

Institute of Immunology and Immunotherapy, University of Birmingham, UK.

Sian Faustini (S)

Institute of Immunology and Immunotherapy, University of Birmingham, UK.

Zehra Yonel (Z)

Periodontal Research Group, School of Dentistry, Institute of Clinical Sciences, University of Birmingham, UK.

Iain L Chapple (IL)

Periodontal Research Group, School of Dentistry, Institute of Clinical Sciences, University of Birmingham, UK.

Mark T Drayson (MT)

Institute of Immunology and Immunotherapy, University of Birmingham, UK.

Alex Richter (A)

Institute of Immunology and Immunotherapy, University of Birmingham, UK.

John P Campbell (JP)

Department for Health, University of Bath, UK.

Jennifer L J Heaney (JLJ)

Institute of Immunology and Immunotherapy, University of Birmingham, UK. Electronic address: j.l.j.heaney@bham.ac.uk.

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Classifications MeSH