tetano
Editor, Senior Moderator
PLoS One
. 2026 Jul 9;21(7):e0353142.
doi: 10.1371/journal.pone.0353142. eCollection 2026.
Full blood count dynamics in immunologically naïve individuals with mild COVID-19: A prospective community cohort study
Seran Hakki[SUP] 1 [/SUP], Sean Nevin[SUP] 1 [/SUP], Emily Conibear[SUP] 1 [/SUP], Kieran J Madon[SUP] 1 [/SUP], Joe Fenn[SUP] 1 [/SUP], Jakob Jonnerby[SUP] 1 [/SUP], Nieves Derqui[SUP] 1 [/SUP], Aleksandra Koycheva[SUP] 1 [/SUP], Rhia Kundu[SUP] 1 [/SUP], Hamish Houston[SUP] 1 [/SUP], Timesh D Pillay[SUP] 1 [/SUP], Alexandra L Kondratiuk[SUP] 1 [/SUP], Janakan Sam Narean[SUP] 1 [/SUP], Kimone L Fisher[SUP] 1 [/SUP], Robert Varro[SUP] 1 [/SUP], Constanta Luca[SUP] 1 [/SUP], Samuel Evetts[SUP] 1 [/SUP], Peter Kelleher[SUP] 2 [/SUP], Onn Min Kon[SUP] 3 [/SUP], Graham P Taylor[SUP] 4 [/SUP], Ajit Lalvani[SUP] 1 [/SUP]
Affiliations
Purpose: Full blood count (FBC) provides a range of cellular haematological parameters and serves as a routinely available basic immune profile. While FBC has been widely used to monitor moderate-to-severe COVID-19 in hospitalised settings, its temporal dynamics in mild, community-managed cases remain poorly characterised, despite these constituting the majority of global infections.
Methods: In a prospective cohort study, we tracked the cellular haematological profiles of 93 recently exposed, immunologically naïve individuals with mild COVID-19 and no underlying co-morbidities, recruited to the Integrated Network for Surveillance, Trials and Investigations into COVID-19 Transmission (INSTINCT) study. Blood samples were collected on D0, D7, D14 and D28 and subsequently aligned to infection-timepoints based on the day of first detected PCR positivity, and analysed using mixed-effects models.
Results: Over 30% of cases exhibited transient, clinically defined neutropenia (mean (95% CI): First PCR-Positive (FP) 2.47x109/L (2.26-2.68) vs convalescence 3.34 x109/L (2.98-3.7); p = 0.0013). Over 20% exhibited lymphopenia (FP 1.38x109/L (1.28-1.48) vs convalescence 1.79x109/L (1.79-2.01); p = 0.0013). Additionally, we observed a notable elevation in platelet count, peaking approximately two weeks after initial infection (mean (95% CI): FP + 14 283x109/L (254-311) vs convalescence 237x109/L (222-252); p = 0.0013).
Conclusions: Transient neutropenia and lymphopenia occurred in approximately one-third and one-fifth of mild COVID-19 cases, respectively, and were followed by a delayed increase in platelet count. This study provides a descriptive, prospective dataset of full blood count parameters spanning early infection to convalescence in immunologically naïve individuals with mild SARS-CoV-2 infection. These data may support mathematical modelling of within-host cellular haematological dynamics and have potential clinical relevance for understanding typical trajectories of routine blood parameters during mild disease.
. 2026 Jul 9;21(7):e0353142.
doi: 10.1371/journal.pone.0353142. eCollection 2026.
Full blood count dynamics in immunologically naïve individuals with mild COVID-19: A prospective community cohort study
Seran Hakki[SUP] 1 [/SUP], Sean Nevin[SUP] 1 [/SUP], Emily Conibear[SUP] 1 [/SUP], Kieran J Madon[SUP] 1 [/SUP], Joe Fenn[SUP] 1 [/SUP], Jakob Jonnerby[SUP] 1 [/SUP], Nieves Derqui[SUP] 1 [/SUP], Aleksandra Koycheva[SUP] 1 [/SUP], Rhia Kundu[SUP] 1 [/SUP], Hamish Houston[SUP] 1 [/SUP], Timesh D Pillay[SUP] 1 [/SUP], Alexandra L Kondratiuk[SUP] 1 [/SUP], Janakan Sam Narean[SUP] 1 [/SUP], Kimone L Fisher[SUP] 1 [/SUP], Robert Varro[SUP] 1 [/SUP], Constanta Luca[SUP] 1 [/SUP], Samuel Evetts[SUP] 1 [/SUP], Peter Kelleher[SUP] 2 [/SUP], Onn Min Kon[SUP] 3 [/SUP], Graham P Taylor[SUP] 4 [/SUP], Ajit Lalvani[SUP] 1 [/SUP]
Affiliations
- PMID: 42424307
- PMCID: PMC13349189
- DOI: 10.1371/journal.pone.0353142
Purpose: Full blood count (FBC) provides a range of cellular haematological parameters and serves as a routinely available basic immune profile. While FBC has been widely used to monitor moderate-to-severe COVID-19 in hospitalised settings, its temporal dynamics in mild, community-managed cases remain poorly characterised, despite these constituting the majority of global infections.
Methods: In a prospective cohort study, we tracked the cellular haematological profiles of 93 recently exposed, immunologically naïve individuals with mild COVID-19 and no underlying co-morbidities, recruited to the Integrated Network for Surveillance, Trials and Investigations into COVID-19 Transmission (INSTINCT) study. Blood samples were collected on D0, D7, D14 and D28 and subsequently aligned to infection-timepoints based on the day of first detected PCR positivity, and analysed using mixed-effects models.
Results: Over 30% of cases exhibited transient, clinically defined neutropenia (mean (95% CI): First PCR-Positive (FP) 2.47x109/L (2.26-2.68) vs convalescence 3.34 x109/L (2.98-3.7); p = 0.0013). Over 20% exhibited lymphopenia (FP 1.38x109/L (1.28-1.48) vs convalescence 1.79x109/L (1.79-2.01); p = 0.0013). Additionally, we observed a notable elevation in platelet count, peaking approximately two weeks after initial infection (mean (95% CI): FP + 14 283x109/L (254-311) vs convalescence 237x109/L (222-252); p = 0.0013).
Conclusions: Transient neutropenia and lymphopenia occurred in approximately one-third and one-fifth of mild COVID-19 cases, respectively, and were followed by a delayed increase in platelet count. This study provides a descriptive, prospective dataset of full blood count parameters spanning early infection to convalescence in immunologically naïve individuals with mild SARS-CoV-2 infection. These data may support mathematical modelling of within-host cellular haematological dynamics and have potential clinical relevance for understanding typical trajectories of routine blood parameters during mild disease.