- Research article
- Open Access
Helminth antigens differentially modulate the activation of CD4+ and CD8+ T lymphocytes of convalescent COVID-19 patients in vitro
BMC Medicine volume 20, Article number: 241 (2022)
The coronavirus disease 2019 (COVID-19) is a respiratory disease caused by SARS-CoV-2, a recently discovered strain of coronavirus. The virus has spread rapidly, causing millions of death worldwide. Contrary to the predictions, prevalence and mortality due to COVID-19 have remained moderate on the African continent. Several factors, including age, genetics, vaccines, and co-infections, might impact the course of the pandemic in Africa. Helminths are highly endemic in Sub-Saharan Africa and are renowned for their ability to evade, skew, and suppress human immune responses through various immune-modulatory mechanisms. Such effects will likely impact SARS-CoV-2 transmission and disease progression.
Here, we analyzed in vitro the impact of antigen extracts from three major helminth parasites, including Onchocerca volvulus, Brugia malayi, and Ascaris lumbricoides, on the immune reactivity to SARS-CoV-2 peptides in COVID-19 patients. Activation of CD4+ and CD8+ T cells was investigated using flow cytometry to monitor the expression of CD137 (4-1BB) and CD69. Cytokine expression, including IL-6, IL-10, IFN-γ, and TNFα, was measured by Luminex in cell culture supernatants.
We observed that helminth antigens significantly reduced the frequency of SARS-CoV-2-reactive CD4+ T helper cells. In contrast, the expression of SARS-CoV-2-reactive CD8+ T cells was not affected and even significantly increased when PBMCs from COVID-19 patients living in Benin, an endemic helminth country, were used. In addition, stimulation with helminth antigens was associated with increased IL-10 and a reduction of IFNγ and TNFα.
Our data offer a plausible explanation for the moderate incidence of COVID-19 in Africa and support the hypothesis that helper T cell-mediated immune responses to SARS-CoV-2 are mitigated in the presence of helminth antigens, while virus-specific cytotoxic T cell responses are maintained.
The coronavirus disease 2019 (COVID-19) is a respiratory disease caused by SARS-CoV-2, a strain of coronavirus initially identified in December 2019 in Wuhan City in China, which can cause severe illness in humans . The virus has spread rapidly, causing millions of death worldwide. Globally, as of April 27t 2022, 508,827,830 confirmed cases of COVID-19, including 6,227,291 deaths, were reported to the WHO . As the pandemic started, WHO predicted millions of COVID-19 deaths in Africa. Contrary to the predictions, 2 years after the first cases, prevalence and mortality have remained surprisingly moderate on the continent . While this has been widely attributed to the younger average age on the continent or the lack of testing capacities, another potential factor might be the co-endemicity of helminths. Indeed, helminth infections, widely spread in Sub-Saharan Africa, are long-lived parasites and renowned for their ability to suppress inflammatory immune reactions to assure persistence in their hosts [4, 5]. Helminths trigger a modified T helper (Th)2 response, where pro-inflammatory components are balanced by regulatory mechanisms including regulatory T and B cells, anti-inflammatory cytokines (IL-10, TGF-β), alternatively activated macrophages, and non-cytolytic antibodies [6,7,8,9]. Clinical manifestations in SARS-CoV-2-infections range from asymptomatic to the devastating acute respiratory distress syndrome (ARDS), where the patients require invasive mechanical ventilation . These severe COVID-19 manifestations have been associated with immunological hyperreactivity characterized by a cytokine storm with high levels of pro-inflammatory cytokines like IL-2, IL-6, IFNγ, and TNFα [11, 12]. Previous data have demonstrated that helminths possess significant immunomodulatory properties that dampen harmful hyperinflammatory responses to viruses, bacteria, and other parasites [13,14,15,16,17,18,19]. In this context, helminth-mediated immune modulation can potentially impact the physiopathology of SARS-CoV-2 infections . Recent reports suggest an inverse correlation between the incidence of COVID-19 and parasitic infections . Following infection with a pathogenic agent, foreign antigens are processed and presented on the surface of antigen-presenting cells with major histocompatibility complex (MHC) molecules to activate T cell receptors . Activated T cells can differentiate into a heterogeneous population of effector T cells, including CD4+ and CD8+ T cells that can mediate pathogen clearance . CD8+ T cells are one of the main components of immunity against intracellular pathogens such as viruses. In contrast, CD4+ T cells are known to help other cells, including cytotoxic T cells and B cells [24, 25]. Upon antigenic activation, T cells upregulate the expression of different markers, including CD69 and CD137 (4-1BB), known as activation-induced markers (AIM). CD137 is a costimulatory member of the TNFR family, expressed on activated CD4+ and CD8+ T cells. CD137 is upregulated 24 h after stimulation on responding T cells regardless of differentiation stage or profile of cytokine secretion . After a peak 24 h after stimulation, CD137 expression gradually declined between 48 and 72 h . CD69 is a membrane-bound, type II C-lectin receptor classically used as an early marker of lymphocyte activation due to its rapid appearance on the surface of the plasma membrane 2–3 h after stimulation . Despite this early apparition, the expression of CD69 peaks between 18 and 24 h after activation before starting to decrease . Emerging data suggest that CD4+ and CD8+ T cell responses play key roles in controlling SARS-CoV-2 infection and COVID-19 [29,30,31].
In the present study, we investigate in vitro the putative impact of helminth co-infection on the activation of SARS-CoV-2-specific T cells in COVID-19 patients by monitoring ex vivo the expression of SARS-CoV-2-induced CD69 and CD137 expression on CD4+ and CD8+ T cells in the presence or absence of helminth antigens. The findings are particularly relevant for developing countries known to be also endemic for helminth parasites.
Study design and clinical characteristics of study participants
The study was conducted between November 2020 and January 2021 and is part of a larger survey. Patients were recruited in Wershofen (Germany) and Zagreb (Croatia). A total of 50 COVID-19 patients (29 men and 21 women) were included in the study. Samples from convalescent COVID-19 donors (N = 6) from Benin, a country endemic for several helminths’ parasites [32,33,34], were collected at the University Hospital of Cotonou as part of an ongoing survey. None of the study participants were vaccinated against COVID-19. Ethical approval for the study was granted by local ethics committees. All included COVID-19 patients had been reported positive by SARS-CoV-2 RT-PCR in official COVID-19 testing centers. Three (6%) out of the 50 COVID-19 patients had been hospitalized during the acute phase of infection. The majority, 41 (82%), had mild symptoms, whereas 6 (12%) were fully asymptomatic (Table 1). Samples from healthy blood donors were kindly provided by the Haematology Department of the University Hospital of Bonn and were used as controls. Healthy blood donors were all negative at SARS-CoV-2 RT-PCR and serology and included 13 men and 17 women (mean age = 32.5 ± 12.37) (Table 1).
Soluble extracts from adult worms of Onchocerca volvulus, Brugia malayi, and Ascaris lumbricoides were prepared as previously described . Briefly, 20 frozen adult worms were thawed and transferred to a Petri dish pre-filled with sterile PBS. Following several washes in PBS, worms were placed inside a glass mortar (VWR, Langenfeld, Germany). Three to 5 ml of RPMI-medium was added, and worms were crushed until a homogenous solution was obtained. The extracts were then centrifuged for 10 min at 300g and 4 °C to remove insoluble material. Supernatants were transferred to a new tube. Protein concentrations were then measured using the Pierce Coomassie Plus (Bradford) Assay Kit (ThermoFisher Scientific, San Diego, CA, USA) according to the manufacturer’s instructions. Aliquots were stored at − 80 °C until use. The optimal concentration for cell stimulation was defined using a titration assay, and the endotoxin level was determined using the Pierce Limulus amoebocyte lysate (LAL) Chromogenic quantification kit (ThermoFisher Scientific). The endotoxin level was routinely below the detection limit of 0.1 EU/ml. Native Influenza A Antigen (H1N1Ag) and Plasmodium falciparum Histidine Rich Protein-2 (PfAg) were obtained from BioRad (Bio-Rad Laboratories GmbH, Feldkirchen, Germany) and used in cell culture at an end concentration of 1 μg/ml.
PBMCs were isolated using a Ficoll gradient as previously described . In brief, 15 ml of heparinized blood was diluted 1:2 in PBS (Gibco, Life Technologies, Carlsbad, USA), transferred on 15 ml of Ficoll (PAN Biotech GmbH, Aidenbach, Germany), and centrifuged for 20 min at 800g, 4 °C and without brake. Cell suspensions were then washed twice, 8 min at 300g, 4 °C, and re-suspended in fetal bovine serum (FBS)-supplemented RPMI 1640 medium (Gibco). The cells were finally counted using the trypan blue (ThermoFisher Scientific) exclusion method and diluted for stimulation and culture.
Stimulation and cell culture
To test the impact of helminth antigens on the immune reactivity to SARS-CoV-2, PBMCs from COVID-19 patients (N = 50) were isolated, and 5 × 106 cells per well were plated and stimulated with SARS-CoV-2-spike-protein-peptide-pools (SPP) (Miltenyi Biotech, Bergisch Gladbach, Germany) at a final concentration of 1 μg/ml, in the presence of culture medium (10% FBS in RPMI) or 10 μg/ml (final concentration) of Brugia malayi, Onchocerca volvulus, or Ascaris lumbricoides extracts. The total volume for each well was adjusted to 250 μl with culture medium (10%FBS in RPMI). Cell culture medium and helminth antigens alone were used as stimulation controls. After 24 h of culture (at 37 °C, 5% CO2), 200 μl supernatants were collected and frozen until use, and cells were harvested and prepared for FACS staining.
All reagents were obtained from ThermoFisher Scientific, and staining was performed according to the manufacturer's instructions. Briefly, cells were harvested and washed with FACS buffer (PBS/2% FBS) at 300 g for 8 min. 1 × 106 cells were then resuspended in 100 μl of FACS buffer and blocked with 1 μl of FC- block (ThermoFisher Scientific) for 15 min. 5 μg/1 × 105 cells of anti-human CD3-PerCP (clone: S4.1-7D6), CD4-eF450 (clone: RPA-T4), CD8-FITC (clone: RPA-T8), CD69-APC (clone: FN50), and CD137-PE (clone: 4B4) were added and the cell suspension was incubated for 30 min at 4 °C. Cells were then washed twice with FACS buffer and fixed in 300 μl PFA (4%). To correct spectral overlaps, fluorescence compensation was done using UltraComp ebeads (ThermoFisher Scientific). Data were acquired using a Cytoflex-S flow cytometer (Beckmann Coulter, Krefeld, Germany) and analyzed with FlowJo v10 software (LLC, Ashland, OR, USA).
The frequency of cells is expressed as the percentage of parent cells (i.e., the frequency of CD4+CD69+ CD137+ T cells is expressed as percentage of the CD4+ T cell population). The gating strategy is shown in Fig. 1. Cells were first gated for lymphocytes by forward and side scatter (FSC-A/SSC-A). A single cell gate was set using FSC-A and FCS-H, and then a gate of viable CD3+ cells was set and used to gate CD4+ and CD8+ T cells. Reactive antigen-specific T cells were gated according to the co-expression of CD137+ and CD69+ in the CD4+ and CD8+ populations.
To quantify cytokine levels in culture supernatants, ProcartaPlex Human Cytokines Panels (ThermoFisher Scientific) were used according to the manufacturer’s instructions. Briefly, anti-IL-6, TNFα, IFNγ, and IL-10-coated magnetic beads were incubated with 25 μl of assay buffer, kit standards, or diluted supernatant (1:2) for 1 h. Twenty-five microliters of biotin-labeled detection antibodies mix was then added. The plates were incubated on an orbital shaker (Stuart, Staffordshire, UK) at 500 rpm for 30 min, and 50 μl of diluted Streptavidin-PE was added. Plates were then incubated for an additional 30 min and washed using a hand-held magnetic plate washer. Afterward, the beads were re-suspended in 120 μl reading buffer. Data were then acquired using a MAGPIX Luminex system and analyzed with ProcartaPlex Analyst software 1.0 (ThermoFisher Scientific).
All graphs were generated using GraphPad Prism 8 (La Jolla, CA, USA). For cell activation data, P values were calculated using the Kruskal-Wallis test. Dunn’s multiple comparison test was used to compare all settings. Significance is accepted if P < 0.05. For cytokine data, Student’s t-test was used for comparisons.
Inhibition of the activation of SARS-CoV-2-reactive CD4+ T cells by helminth antigens in COVID-19 patients
To determine whether and how CD4+ helper T cell activation by SARS-CoV-2 peptides is affected by the presence of helminth antigens, we examined the frequency of activated CD4+ T cells expressing simultaneously CD69 and CD137 in PBMCs of convalescent COVID-19 patients following stimulation with SARS-CoV-2 peptides alone (SPP), or in combination with helminth antigens (OvAg, BmAg or AlAg). As shown in Fig. 2, the frequency of double-positive CD4+ T cells expressing CD69 and CD137 was significantly increased after stimulation with SPP (Fig. 2A, B). In the presence of helminth antigens alone, no significant T cell activation was seen (Fig. 2C–E). The frequency of helper T cells expressing CD69 and CD137 was significantly decreased in PBMCs stimulated with SPP in the presence of helminth antigens (Fig. 2F, G and I–K). Similarly, the helminth antigens also inhibited SARS-CoV-2-specific T cell activation when samples from convalescent COVID-19 patients from helminth endemic region in Benin were used (Additional file 1, Fig. S1).
No suppression of the activation of SARS-CoV-2-reactive CD8+ T cells by helminth antigens in COVID-19 patients
To determine whether the inhibition of CD4+ helper T cells activation also applies to CD8+ cytotoxic T cells, we investigated the expression of CD69+CD137+ in the CD8+ T cell population. SPP induced, as described above, a significant increase in the activation of SARS-CoV-2-specific cytotoxic T cells (Fig. 3A, B). Helminth antigens OvAg (Fig. 3C), BmAg (Fig. 3D), and AlAg (Fig. 3E) induced no significant increase in the expression of CD69 and CD137 double-positive CD8+ T cells. In contrast to the observations in the CD4+ T cell population, the frequency of SARS-CoV-2-reactive CD8+ T cells was not affected by the presence of helminth antigens (Fig. 3F–H and I–K). More interestingly, helminth antigens induced a significant increase of SARS-CoV-2-specific CD8+ T cells when PBMCs from convalescent COVID-19 patients from endemic helminth region in Benin were used (Additional file 2: Fig. S2).
Modulation of SARS-CoV-2-reactive CD4+ and CD8+ T cells is associated with an increase of IL-10
To explore the mechanisms associated with this immune suppression by helminth antigens, we analyzed cytokine expression in culture supernatants using a Luminex-based multiplex immunoassay. Indeed, in wells stimulated with SPP in the presence of OvAg, BmAg, or AlAg, significantly higher levels of IL-10 were detected compared to wells stimulated SPP alone (Fig. 3A–C). Interestingly, while a non-significant increase of IL-6 was seen in the presence of OvAg and BmAg, significance was reached in the presence of AlAg (Fig. 4D–F). Moreover, a significant reduction of SPP-induced IFNγ and TNFα expression was seen in the presence of OvAg or BmAg, while a robust trend was observed in the presence of AlAg (Fig. 4G–L).
No impact of H1N1 and Plasmodium falciparum antigens on the frequencies of SARS-CoV-2-reactive CD4+ and CD8+ T cells in COVID-19 patients
To determine whether the observed modulation of CD4+ and CD8+ T cells is specific to helminth antigens, we investigated the effects of Native Influenza A Antigen (H1N1Ag) and Plasmodium falciparum Histidine Rich Protein-2 (PfAg) in the same settings. As shown in Fig. 5, H1N1Ag and PfAg alone induced no significant T cell activation (Fig. 5A–D). After co-stimulation with SPP and H1N1Ag on the one hand and SPP and PfAg on the second, neither H1N1Ag nor PfAg significantly affected the expression of SARS-CoV-2-reactive CD4+ T helper T cells (Fig. 5E–F and G–H). Similar data were obtained when CD8+ T cells were analyzed (Additional file 3: Fig. S3)
Our data support the hypothesis that in the presence of helminth antigens, immune responses to SARS-CoV-2 are mitigated with regard to CD4+ T cells and pro-inflammatory cytokine responses. In contrast, SARS-CoV-2-reactive CD8+ T cell responses are maintained in COVID-19 patients and even increased when helminth endemic samples were used. This may critically shift the overall immune response to SARS-CoV-2 such that overreaction and severe COVID-19 are avoided, similar to helminths’ ability to mitigate systemic inflammatory response syndrome in animal models and in humans [36, 37].
Even though a role for helminth-induced T cell-intrinsic regulation mechanisms, such as anergy, adaptive tolerance, exhaustion, or plasticity, cannot be excluded, the most probable mechanism for this helminth-induced modulation of T cells might involve innate cells. Indeed, our data indicate that helminth antigens alone do not directly activate T cells. Knowing that CD8+ T cells require CD4+ T cell help for full activation [38,39,40], it may seem unexpected that CD8+ T cells get activated when CD4+ T cells are suppressed. However, even though CD4+ T cells are necessary for the development of functional memory CD8+ T cells, their requirement for the induction of a primary CD8+ T cell response following infection is less clear . Emerging data suggest that Toll-like receptor (TLR) stimulation can bypass the requirement for CD4+ T cell help following immunization . These data, together with the fact that helminth antigens are known to activate TLRs  offer a possible mechanism for the differential modulation of CD4+ and CD8+ observed in our study.
The cytokine data suggest that increased IL-10 expression is associated with helminth-induced suppression of antigen-specific CD4+ T cell activation. A moderate increase in IL-6 expression was seen only in the presence of AlAg. The differences in IL-6 expression to the controls were, however, not significant, suggesting a key role for IL-10, but no significant part played by IL-6 in the observed modulations.
In our setting, helminth antigens also inhibited SPP-induced expression of Th1 cytokines, including IFNγ and TNFα. The increase of IL-10 might directly induce the suppression of Th1 cytokines, as previously described . Indeed, IL-10 is considered as a potent immune regulatory cytokine . Even though our data did not clarify the origin of IL-10, it can be considered that antigen-presenting cells, chiefly monocytes are the main source of IL-10 in our setting due to the short incubation period. Indeed, monocytes have been defined as the major source of IL-10 in peripheral blood cells [43, 45]. In addition, helminth-induced alternative maturation of monocytes might influence T cell activation .
Moreover, IL-10 was shown in other parasitic infections to contribute to the expansion and functional activation of CD8+ T cells . In a rodent model, it was demonstrated that antitumor therapy combining IL-10 and oncolytic adenovirus Ad-hTERT increased CD8+ T cell-dependent antitumor efficacy . Altogether, these data, in combination with our current finding, suggest a key role for IL-10 in both the suppression of SARS-CoV-2-specific CD4+ T cells and the activation or maintenance of CD8+ T cells.
Our results with H1N1Ag or PfAg further support the hypothesis that the observed modulation of SARS-CoV-2-reactive CD4+ and CD8+ T cells in samples from COVID-19 patients is associated with helminth intrinsic immune regulatory properties. Additional data are still required to better define the associated mechanisms.
Our data confirm hypotheses formulated by others, suggesting that helminth parasites and their derivatives might exert an anti-pathological effect in COVID-19 patients  and contradict speculations staging helminths as potential potentiators of COVID-19-related morbidity and mortality through suppression of efficient immune response against SARS-CoV-2 [50, 51]. Indeed, despite the implication of Th2 responses in the cytokine storm responsible for the pathology of COVID-19 , the typical helminth-induced Th2 immune response is associated with a strong regulatory arm that might significantly mitigate COVID-19 severity [6, 7]. The helminth-induced maintenance or increase of SARS-CoV-2-specific cytotoxic T cells activation observed in samples from COVID-19 patients in our study may be the key element that facilitates the elimination of SARS-CoV-2-infected cells.
The major limitation of the present study is the fact that most samples were collected in Europe. It cannot be excluded that samples from helminth endemic regions react differently. However, samples from 6 convalescent COVID-19 patients obtained from Benin, a country endemic to several helminth parasites [32, 52] were largely in line with the data obtained using European samples. Interestingly, while the helminth antigens did not affect the activation of CD8+ T cells in European samples, a significant increase in the activation of CD8+ T cells was seen in the Benin samples when PBMCs were stimulated simultaneously with helminth antigens and SARS-CoV-2 peptides.
Even though several other factors might be involved in the low incidence of COVID-19 in helminth endemic countries, and additional data are still required to understand the mechanisms, our current data offer a proof of principle and one plausible explanation for why African countries, endemic for helminth parasites are moderately affected by the COVID-19 pandemic . This differential helminth-induced immunomodulation of CD4+ and CD8+ T cells might also be relevant to the immunogenicity of current COVID-19 vaccines in endemic helminth regions. Indeed, it is unclear if helminth-induced immunomodulation, as recently hypothesized by Chacin-Bonilla et al. , would affect the efficacy of COVID-19 vaccines in helminth endemic regions.
The present study uniquely demonstrates that antigens from three major helminth parasites (Brugia malayi, Onchocerca volvulus, and Ascaris lumbricoides) could potentially modulate the immune reactivity to SARS-CoV-2 peptides by suppressing reactive CD4+ helper T cells while maintaining SARS-CoV-2 reactive CD8+ cytotoxic T cells. This finding offers a plausible explanation for the moderate incidence of COVID-19 in helminth endemic countries and opens new research avenues into the impact of helminth-induced immune-regulation on the COVID-19 disease outcome and vaccination effectiveness in tropical countries.
Availability of data and materials
All data used for the study are included in the manuscript and the supplementary materials. Additional data related to the work may be available upon request.
Adenovirus-human telomerase reverse transcriptase
Ascaris lumbricoides antigen
Acute respiratory distress syndrome
Brugia malayi antigen
Cluster of differentiation
Coronavirus disease 2019
Fluorescence-activated cell sorting
Fetal bovine serum
- FC- block:
Fragment crystallizable region blocking solution
- FSC- (A/H):
Flu virus H1N1 (hemagglutinin1, neuraminidase1) antigen
Limulus amoebocyte lysate
Major histocompatibility complex
Onchocerca volvulus antigen
Peripheral Blood Mononuclear Cell
Plasmodium falciparum antigen
Rotation per minute
Roswell Park Memorial Institute
Severe acute respiratory syndrome coronavirus type 2
Standard error of mean
Transforming growth factor-beta
Tumor necrosis factor
Tumor necrosis factor receptor
World Health Organization
WHO. Coronavirus disease (COVID-19) pandemic 2022 [Available from: https://www.euro.who.int/en/health-topics/health-emergencies/coronavirus-covid-19/novel-coronavirus-2019-ncov]. Accessed 27 Apr 2022.
WHO. WHO Coronavirus (COVID-19) Dasboard 2022 [Available from: https://covid19.who.int]. Accessed 27 Apr 2022.
Mbow M, Lell B, Jochems SP, Cisse B, Mboup S, Dewals BG, et al. COVID-19 in Africa: dampening the storm? Science. 2020;369(6504):624–6.
Harris NL, Loke P. Recent advances in type-2-cell-mediated immunity: insights from helminth infection. Immunity. 2018;48(2):396.
email@example.com C-CRCEa. Global coalition to accelerate COVID-19 clinical research in resource-limited settings. Lancet. 2020;395(10233):1322–5.
Maizels RM, McSorley HJ. Regulation of the host immune system by helminth parasites. J Allergy Clin Immunol. 2016;138(3):666–75.
Adjobimey T, Hoerauf A. Induction of immunoglobulin G4 in human filariasis: an indicator of immunoregulation. Ann Trop Med Parasitol. 2010;104(6):455–64.
Satoguina JS, Adjobimey T, Arndts K, Hoch J, Oldenburg J, Layland LE, et al. Tr1 and naturally occurring regulatory T cells induce IgG4 in B cells through GITR/GITR-L interaction, IL-10 and TGF-beta. Eur J Immunol. 2008;38(11):3101–13.
Adjobimey T, Hoerauf A. Distinct N-linked immunoglobulin G glycosylation patterns are associated with chronic pathology and asymptomatic infections in human lymphatic filariasis. Front Immunol. 2022;13:790895.
Badraoui R, Alrashedi MM, El-May MV, Bardakci F. Acute respiratory distress syndrome: a life threatening associated complication of SARS-CoV-2 infection inducing COVID-19. J Biomol Struct Dyn. 2020;39(17):6842–51.
Melo AKG, Milby KM, Caparroz A, Pinto A, Santos RRP, Rocha AP, et al. Biomarkers of cytokine storm as red flags for severe and fatal COVID-19 cases: A living systematic review and meta-analysis. PLoS One. 2021;16(6):e0253894.
Mehta P, Fajgenbaum DC. Is severe COVID-19 a cytokine storm syndrome: a hyperinflammatory debate. Curr Opin Rheumatol. 2021;33(5):419–30.
Arndts K, Deininger S, Specht S, Klarmann U, Mand S, Adjobimey T, et al. Elevated adaptive immune responses are associated with latent infections of Wuchereria bancrofti. PLoS Negl Trop Dis. 2012;6(4):e1611.
Ritter M, Osei-Mensah J, Debrah LB, Kwarteng A, Mubarik Y, Debrah AY, et al. Wuchereria bancrofti-infected individuals harbor distinct IL-10-producing regulatory B and T cell subsets which are affected by anti-filarial treatment. PLOS Negl TropDis. 2019;13(5):e0007436.
Ritter M, Ndongmo WPC, Njouendou AJ, Nghochuzie NN, Nchang LC, Tayong DB, et al. Mansonella perstans microfilaremic individuals are characterized by enhanced type 2 helper T and regulatory T and B cell subsets and dampened systemic innate and adaptive immune responses. PLoS Negl Trop Dis. 2018;12(1):e0006184.
Kroidl I, Chachage M, Mnkai J, Nsojo A, Berninghoff M, Verweij JJ, et al. Wuchereria bancrofti infection is linked to systemic activation of CD4 and CD8 T cells. PLoS Negl Trop Dis. 2019;13(8):e0007623.
Hübner MP, Layland LE, Hoerauf A. Helminths and their implication in sepsis - a new branch of their immunomodulatory behaviour? Pathog Dis. 2013;69(2):127–41.
Loffredo-Verde E, Bhattacharjee S, Malo A, Festag J, Kosinska AD, Ringelhan M, et al. Dynamic, helminth-induced immune modulation influences the outcome of acute and chronic hepatitis B virus Infection. J Infect Dis. 2020;221(9):1448–61.
Colombe S, Machemba R, Mtenga B, Lutonja P, Kalluvya SE, de Dood CJ, et al. Impact of schistosome infection on long-term HIV/AIDS outcomes. PLoS Negl Trop Dis. 2018;12(7):e0006613.
Bradbury RS, Piedrafita D, Greenhill A, Mahanty S. Will helminth co-infection modulate COVID-19 severity in endemic regions? Nat Rev Immunol. 2020;20(6):342.
Gutman JR, Lucchi NW, Cantey PT, Steinhardt LC, Samuels AM, Kamb ML, et al. Malaria and parasitic neglected tropical diseases: potential syndemics with COVID-19? Am J Trop Med Hyg. 2020;103(2):572–7.
Hwang JR, Byeon Y, Kim D, Park SG. Recent insights of T cell receptor-mediated signaling pathways for T cell activation and development. Exp Mol Med. 2020;52(5):750–61.
Laidlaw BJ, Craft JE, Kaech SM. The multifaceted role of CD4(+) T cells in CD8(+) T cell memory. Nat Rev Immunol. 2016;16(2):102–11.
Pusnik J, Richter E, Schulte B, Dolscheid-Pommerich R, Bode C, Putensen C, et al. Memory B cells targeting SARS-CoV-2 spike protein and their dependence on CD4(+) T cell help. Cell Rep. 2021;35(13):109320.
Zander R, Schauder D, Xin G, Nguyen C, Wu X, Zajac A, et al. CD4(+) T cell help is required for the formation of a cytolytic CD8(+) T cell subset that protects against chronic infection and cancer. Immunity. 2019;51(6):1028–42 e4.
Wolfl M, Kuball J, Ho WY, Nguyen H, Manley TJ, Bleakley M, et al. Activation-induced expression of CD137 permits detection, isolation, and expansion of the full repertoire of CD8+ T cells responding to antigen without requiring knowledge of epitope specificities. Blood. 2007;110(1):201–10.
Cibrian D, Sanchez-Madrid F. CD69: from activation marker to metabolic gatekeeper. Eur J Immunol. 2017;47(6):946–53.
Testi R, D'Ambrosio D, De Maria R, Santoni A. The CD69 receptor: a multipurpose cell-surface trigger for hematopoietic cells. Immunol Today. 1994;15(10):479–83.
Fong SW, Yeo NK, Chan YH, Goh YS, Amrun SN, Ang N, et al. Robust virus-specific adaptive immunity in COVID-19 patients with saRS-CoV-2 Delta382 variant infection. J Clin Immunol. 2022;42(2):214–29.
Rydyznski Moderbacher C, Ramirez SI, Dan JM, Grifoni A, Hastie KM, Weiskopf D, et al. Antigen-specific adaptive immunity to SARS-CoV-2 in acute COVID-19 and associations with age and disease severity. Cell. 2020;183(4):996–1012 e19.
Sette A, Crotty S. Adaptive immunity to SARS-CoV-2 and COVID-19. Cell. 2021;184(4):861–80.
Boko-Collins PM, Ogouyemi-Hounto A, Adjinacou-Badou EG, Gbaguidi-Saizonou L, Dossa NI, Dare A, et al. Assessment of treatment impact on lymphatic filariasis in 13 districts of Benin: progress toward elimination in nine districts despite persistence of transmission in some areas. Parasit Vectors. 2019;12(1):276.
Gyapong JO, Kyelem D, Kleinschmidt I, Agbo K, Ahouandogbo F, Gaba J, et al. The use of spatial analysis in mapping the distribution of bancroftian filariasis in four West African countries. Ann Trop Med Parasitol. 2002;96(7):695–705.
Avokpaho E, Houngbegnon P, Accrombessi M, Atindegla E, Yard E, Rubin Means A, et al. Factors associated with soil-transmitted helminths infection in Benin: Findings from the DeWorm3 study. PLoS Negl Trop Dis. 2021;15(8):e0009646.
Prodjinotho UF, von Horn C, Debrah AY, Batsa Debrah L, Albers A, Layland LE, et al. Pathological manifestations in lymphatic filariasis correlate with lack of inhibitory properties of IgG4 antibodies on IgE-activated granulocytes. PLoS Negl Trop Dis. 2017;11(7):e0005777.
Gondorf F, Berbudi A, Buerfent BC, Ajendra J, Bloemker D, Specht S, et al. Chronic filarial infection provides protection against bacterial sepsis by functionally reprogramming macrophages. PLoS Pathog. 2015;11(1):e1004616.
Panda M, Sahoo PK, Mohapatra AD, Dutta S, Thatoi PK, Tripathy R, et al. Decreased prevalence of sepsis but not mild or severe P. falciparum malaria is associated with pre-existing filarial infection. Parasit Vectors. 2013;6:203.
Frank GM, Lepisto AJ, Freeman ML, Sheridan BS, Cherpes TL, Hendricks RL. Early CD4(+) T cell help prevents partial CD8(+) T cell exhaustion and promotes maintenance of Herpes Simplex Virus 1 latency. J Immunol. 2010;184(1):277–86.
Lu YJ, Barreira-Silva P, Boyce S, Powers J, Cavallo K, Behar SM. CD4 T cell help prevents CD8 T cell exhaustion and promotes control of Mycobacterium tuberculosis infection. Cell Rep. 2021;36(11):109696.
Cullen JG, McQuilten HA, Quinn KM, Olshansky M, Russ BE, Morey A, et al. CD4(+) T help promotes influenza virus-specific CD8(+) T cell memory by limiting metabolic dysfunction. Proc Natl Acad Sci U S A. 2019;116(10):4481–8.
Hervas-Stubbs S, Olivier A, Boisgerault F, Thieblemont N, Leclerc C. TLR3 ligand stimulates fully functional memory CD8+ T cells in the absence of CD4+ T-cell help. Blood. 2007;109(12):5318–26.
Sun S, Wang X, Wu X, Zhao Y, Wang F, Liu X, et al. Toll-like receptor activation by helminths or helminth products to alleviate inflammatory bowel disease. Parasit Vectors. 2011;4:186.
Prasse A, Germann M, Pechkovsky DV, Markert A, Verres T, Stahl M, et al. IL-10-producing monocytes differentiate to alternatively activated macrophages and are increased in atopic patients. J Allergy Clin Immunol. 2007;119(2):464–71.
Rasquinha MT, Sur M, Lasrado N, Reddy J. IL-10 as a Th2 cytokine: differences between mice and humans. J Immunol. 2021;207(9):2205–15.
de Waal MR, Abrams J, Bennett B, Figdor CG, de Vries JE. Interleukin 10(IL-10) inhibits cytokine synthesis by human monocytes: an autoregulatory role of IL-10 produced by monocytes. J Exp Med. 1991;174(5):1209–20.
Semnani RT, Mahapatra L, Moore V, Sanprasert V, Nutman TB. Functional and phenotypic characteristics of alternative activation induced in human monocytes by interleukin-4 or the parasitic nematode Brugia malayi. Infect Immun. 2011;79(10):3957–65.
Pino-Martinez AM, Miranda CG, Batalla EI, Gonzalez-Cappa SM, Alba Soto CD. IL-10 participates in the expansion and functional activation of CD8(+) T cells during acute infection with Trypanosoma cruzi. J Leukoc Biol. 2019;105(1):163–75.
Chen D, Huang L, Zhou H, Zhang Y. Combining IL-10 and oncolytic adenovirus demonstrates enhanced antitumor efficacy through CD8(+) T cells. Front Immunol. 2021;12:615089.
Siles-Lucas M, Gonzalez-Miguel J, Geller R, Sanjuan R, Perez-Arevalo J, Martinez-Moreno A. Potential influence of helminth molecules on COVID-19 pathology. Trends Parasitol. 2021;37(1):11–4.
Abdoli A. Helminths and COVID-19 co-infections: a neglected critical challenge. ACS Pharmacol Transl Sci. 2020;3(5):1039–41.
Chacin-Bonilla L, Chacon-Fonseca N, Rodriguez-Morales AJ. Emerging issues in COVID-19 vaccination in tropical areas: impact of the immune response against helminths in endemic areas. Travel Med Infect Dis. 2021;42:102087.
Ibikounle M, Onzo-Aboki A, Doritchamou J, Tougoue JJ, Boko PM, Savassi BS, et al. Results of the first mapping of soil-transmitted helminths in Benin: evidence of countrywide hookworm predominance. PLoS Negl Trop Dis. 2018;12(3):e0006241.
We thank all of the study participants, the teams of the Laboratory of Cytogenetics, and the Biochemistry and Molecular Biology Unit of the University of Abomey-Calavi in Benin for providing samples from endemic controls and the Institute of Hematology of the University Hospital of Bonn in Germany for providing samples from healthy donors.
Open Access funding enabled and organized by Projekt DEAL. - AH is funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany’s Excellence Strategy—EXC2151—390873048.
- The funders had no role in study design, data collection, analysis, decision to publish, or manuscript preparation.
Ethics approval and consent to participate
Each volunteer recruited for the study gave informed consent to participate. Ethics approval for the study was obtained from the ethical boards of the University Hospital Bonn in Germany (Lfd.Nr.439/20), the Zadar General Hospital in Croatia (02-3534/20-2/20), and the Ethics Committee for Biomedical Research of the University of Parakou in Benin (0458/CLERB-UP/P/SP/R/SA).
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
. Inhibition of SARS-CoV-2-reactive CD4+ T cells by helminth antigens in COVID-19 patients from a helminth endemic region. Graph summarizes the frequencies of CD69+ and CD137+ in CD4+ T cells in the different settings. Each symbol represents individual donors. Bars indicate Means ± SEM of the percentage of SARS-CoV-2-reactive T cells. Data were obtained from 6 COVID-19 patients in Benin.
. Enhancement of the activation of SARS-CoV-2-specific CD8+ T cells by helminth antigens in COVID-19 patients from a helminth endemic region. Graph summarizes the frequencies of CD69+ and CD137+ in CD8+ T cell populations in the different settings. Each symbol represents individual donors. Bars indicate Means ± SEM of the percentage of SARS-CoV-2-reactive T cells in each setting. Data were obtained from 6 COVID-19 patients in Benin.
. No modulation of SARS-CoV-2-specific CD8+ T cells by helminth antigens in COVID-19 patients. Graphs summarize the frequencies of CD69+ and CD137+ in CD8+ T cell populations in the different settings in the presence of H1N1Ag (A) or PfAg (B). Each symbol represents individual donors. Bars indicate Means ± SEM of the percentage of SARS-CoV-2-reactive T cells in each setting. Data were obtained from 15 COVID-19 patients.
About this article
Cite this article
Adjobimey, T., Meyer, J., Terkeš, V. et al. Helminth antigens differentially modulate the activation of CD4+ and CD8+ T lymphocytes of convalescent COVID-19 patients in vitro. BMC Med 20, 241 (2022). https://doi.org/10.1186/s12916-022-02441-x
- Helminth antigens
- CD4+ helper and CD8+ T cytotoxic T cells
- activation markers
- CD137 (4-1BB)