Skip to main content

Primary Toxoplasma gondii infection-associated with hemophagocytic syndrome in a man with HIV infection: a case report

Abstract

Background

Reactivation of latent Toxoplasma gondii (T. gondii) infection is more common than primary infection in patients with human immunodeficiency virus (HIV). We report a rare case of primary T. gondii infection-associated hemophagocytic syndrome (HPS).

Case presentation

A man with HIV infection presented with fever, dyspnea and pancytopenia. He was diagnosed with primary T. gondii infection by the seroconversion from single-positive IgM antibody to double-positive IgM and IgG antibody. Metagenomic next-generation sequencing (mNGS) of a plasma sample yielded high reads of T. gondii DNA. He responded well to combined anti-Toxoplasma medicines and glucocorticoid treatment.

Conclusions

In patients with HPS and positive T. gondii IgM antibody, mNGS analysis of a peripheral blood sample is helpful in diagnosing disseminated T. gondii infection. The dynamic changes by serological detection for IgM and IgG of T. gondii further supported the inference that the patient has experienced a primary T. gondii infection.

Peer Review reports

Background

In individuals with human immunodeficiency virus (HIV) infection, reactivation of latent Toxoplasma gondii (T. gondii) infection is more common than primary infection [1]. Primary T. gondii infection is usually asymptomatic. The central nervous system is mostly affected in a T. gondii reactivation infection. Cases of hemophagocytic syndrome (HPS) associated with disseminated toxoplasmosis infection have been reported among transplant recipients and immune competent adults [2, 3]. Among individuals with HIV infection, the major causes of HPS are infection with Mycobacterium, Cytomegalovirus, Cryptococcus neoformans, and hematological or tumoral disease [4]. However, cases of primary T. gondii infection-associated HPS have not been reported in HIV-infected individuals. Here, we described a man with HIV infection and HPS, who was ultimately diagnosed with primary T. gondii infection.

Case presentation

A 33-year-old Chinese man with HIV infection was admitted to our hospital on October 30, 2019. The patient presented a 15-day history of sustained fever (the highest temperature was 39 ℃), followed by 2 days of dyspnea but without impaired consciousness, headache, rash and weight loss. He had been previously diagnosed with HIV infection and had been taking antiretroviral therapy (ART) with a regimen of lamivudine, tenofovir, and efavirenz for 6 years. He reported that his CD4 + T-cell count had increased from 100 to 200 cells/μL 2 years previously.

Chest computed tomography (CT) showed thickened bronchial walls with surrounding interstitium in both lungs, double-track signs, thickened interlobular septa, multiple ground-glass opacities in the periphery of both lungs, widened pulmonary artery segment, a small amount of pleural effusion on both sides and pericardial effusion. Abdomen CT showed severe fatty liver and splenomegaly (Fig. 1A–H). No abnormalities were detected on contrast magnetic resonance imaging (MRI) of the brain.

Fig. 1
figure 1

Presentation of Chest and Abdomen computed tomography (CT) findings. Chest CT showed thickened bronchial walls with surrounding interstitium in both lungs, double-track signs (A), thickened interlobular septa, multiple ground-glass opacities in the periphery of both lungs (BE), widened pulmonary artery segment (F), a small amount of pleural effusion on both sides and pericardial effusion (G). Abdomen CT showed severe fatty liver and splenomegaly (H). After 2-week chest CT indicated significant improvement of pulmonary lesions (IM), normal pulmonary artery segment is visible (N), pleural effusion and pericardial effusion disappeared (O), fatty liver and normal spleen (P)

Laboratory results revealed normal leukocyte count, decreased platelet count (52 × 109/L), mild anemia (99 g/L), elevated level of C-reactive protein (104.5 mg/L), glutamic amino transferase (121 U/L), aspartate amino transferase (193 U/L), lactic dehydrogenase (LDH) (above 4300 U/L), and a normal galactomannan level. His CD4 + T-cell and CD8 + T-cell counts were only 8 cells/μL and 510 cells/μL, respectively. Arterial blood gas analysis revealed hypoxemia (arterial oxygen tension 55.2 mmHg). He tested negative for the serum cryptococcal antigen test, and IgM antibodies to herpes simplex virus, Epstein-Barr virus (EBV), and cytomegalovirus (CMV), but was positive for IgG antibodies. The EBV and CMV DNA in the peripheral blood were undetectable. Three sets of blood cultures for bacteria and fungi were negative.

The patient was positive for T. gondii IgM antibody (9.82 AU/mL; reference range: 0–6 AU/mL) (TOXM0460DS/96Wells, ELISA, DiaSorin) and negative for IgG antibody (7.04 IU/mL; reference range: 0–7.2 IU/mL) (TOXG0460DS/96Wells, ELISA, DiaSorin). The HIV RNA load was 3.1 × 105 copies/mL and drug resistances were detected. His acute respiratory failure was assumed to be caused by Pneumocystis jirovecii (P. jirovecii) pneumonia (PJP). After 5 days treatment with sulfamethoxazole (SMZ; 15 mg/kg/day), trimethoprim (TMP; 15 mg/kg/day), and methylprednisolone (80 mg/day), his fever and dyspnea showed no improvement. Subsequently, a diagnosis of HPS was considered based on the following criteria: sustained fever; pancytopenia (leukocyte count: 2.51 × 109/L, platelet count: 9 × 109/L, hemoglobin: 8.5 g/dL); elevated levels of sCD25 (1485 U/mL; reference range: 223–710 U/mL), serum ferritin (> 2000 μg/L), and triglyceride (4.74 mmol/L); splenomegaly; and a decreased CD16 + CD56 + T-cell count (58 cells/μL; reference range: 90–590 cells/μL). Two attempts of bone marrow biopsy failed to obtain any bone marrow components. A plasma sample was sent to BGI PathoGenesis Pharmaceutical Technology (BGI-Shenzhen) for metagenomic next-generation sequencing (mNGS), which indicated T. gondii infection (Fig. 2).The patient was treated with a 5-day course of human immunoglobulin (0.4 g/kg/day) and combined therapy of SMZ-TMP, clindamycin and methylprednisolone. The ART drugs were changed to a regimen of lopinavir/ritonavir and dolutegravir sodium. A week later, fever and dyspnea were relieved, his platelet count recovered to 50 × 109/L, serum T. gondii IgM antibody had increased to 12 AU/mL and IgG antibody had turned positive (7.49 AU/mL), which confirmed the diagnosis of primary T. gondii infection associated HPS. Two weeks later, his chest CT showed significant improvement (Fig. 1I–P). After 6 weeks of treatment, his red blood cell count had returned to normal. Four months later, T. gondii IgM antibody increased to over 160 AU/mL and IgG antibody increased to > 400 AU/mL. The CD4 + T-cell count was 169 cells/μL, CD8 + T-cell count was 2540 cells/μL, and HIV RNA load was 35 copies/mL.

Fig. 2
figure 2

Pathogen identification from blood samples using next-generation sequencing method. The number of sequencing mapped reads that corresponded to T. gondii was 7017 (91.06%) (A) with 0.44514% genome coverage (B). Reads distribution of total DNA sequence in the sample was without the human host

Discussion and conclusion

This was a rare case of primary T. gondii infection in an AIDS patient with HPS who previously experienced virological and immunological failure and had not been administered primary prophylaxis with SMZ-TMP. We were unable to find any published reports of primary T. gondii infection with HPS in patients with HIV. The primary T. gondii infection was initially identified based on the seroconversion from single-positive IgM antibody to double-positive IgM and IgG antibodies. However, the sensitivity, specificity and positive predictive values of IgM antibody by enzyme-linked immune sorbent assay for acute toxoplasmosis infection have been reported to be 98.1%, 65.0% and 43.3%, respectively [5]. False positive T. gondii IgM antibody can occur due to cross-reactivity with various autoimmune antibodies [6], while false negative T. gondii IgG antibody can occur in immune compromised individuals [7]. The diagnosis of disseminated T. gondii infection was subsequently confirmed by mNGS of a plasma sample. To our knowledge, only two cases HIV-infected patients with T. gondii infection-associated HPS have previously been reported, and both were due to reactivated T. gondii infection with positive IgG and negative IgM antibodies [8, 9]. Reactivation of latent T. gondii infection is more common than primary infection in patients with HIV, and most reported cases of primary T. gondii infection were from kidney transplant recipients [2]. In HIV-infected individuals, regardless of their immune status, primary T. gondii infection is generally asymptomatic [4, 10, 11], although some reported manifestations of macular rash [12] or acute respiratory distress [13]. In China the seroprevalence of T. gondii infection was 8.2% from 2000 to 2007, but has increased in recent years [14]. The prevalence of T. gondii IgG antibody in individuals with HIV infection has been reported to be higher than that of healthy controls (9.7% vs. 4.7%), while the seroprevalences of Toxoplasma IgM antibody is similar in both groups [15].In this patient, the level of T. gondii IgM and IgG antibodies increased greatly in the convalescent period. Generally, T. gondii antibody levels returned to normal within 4–6 months; however, some cases reported persistence of positive T. gondii IgM longer than 1 year. In this case, the delayed disappearance of T. gondii IgM antibody may be associated with obvious immune function restoration from HPS and virological control after adjusting the regimen of ART. Notably, serum T. gondii antibodies were only tested at baseline, 1 week, and at 4 months, possibly missing the peak level of T. gondii IgM antibody.

The lung is the second most common site of T. gondii infection. In transplant recipients and individuals with HIV infection, respiratory manifestations of acute toxoplasmosis usually present as a subacute febrile illness with cough and dyspnea. Patients with T. gondii pneumonia have significantly higher LDH levels than those with PJP. The diagnosis of pulmonary toxoplasmosis is challenging due to the nonspecific nature of clinical and radiographic findings. Chest CT may reveal centrilobular patchy or diffuse ground-glass opacities resembling PJP. Extrapulmonary involvement may be present in the liver, brain, bone marrow, heart, and stomach. Pulmonary coinfection of T. gondii and P. jirovecii has been reported [16]. Although no bronchoalveolar lavage fluid (BALF) specimen was tested in this case, the blood mNGS did not detect P. jirovecii, suggesting that the patient had T. gondii monoinfection without P. jirovecii coinfection.

Based on the brain MRI, neurological manifestations and lesions were not obsverved in the patient. In patients with toxoplasmic encephalitis (TE), MRI commonly shows one or more focal ring-enhancing mass lesions, but TE can manifest as diffuse encephalitis or ventriculitis. Moreover, there have been reports of unmasking and paradoxical TE immune reconstitution inflammatory syndrome after initiating ART in patients with HIV infection [17, 18].

Among different specimens, hematoxylin and eosin stainings, immunoperoxidase staining, and polymerase chain reaction (PCR) can be used for the detection of T. gondii. However, PCR detection for T. gondii was unavailable in our hospital. In this patient, cerebrospinal fluid (CSF), bone marrow specimen, and BALF specimen were not obtained. Patients with TE can be diagnosed by mNGS using CSF specimen [19]. However, to our knowledge, there have been no previous reports of mNGS being used to diagnose toxoplasmosis using a peripheral blood sample.

In summary, T. gondii infection-associated HPS can occur in primary and reactivated latent infection. The application of mNGS analysis using a peripheral blood sample could help in the diagnosis of T. gondii infection when it is difficult to obtain optimal specimens. Early diagnosis and treatment with the combination of anti-Toxoplasma and glucocorticoid medications can help in achieving favorable outcomes. In T. gondii seronegative patients with severe immunodeficiency, prevention of primary infection using SMZ-TMP prophylaxis is recommended.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.

Abbreviations

ART:

Antiretroviral treatment

BALF:

Bronchoalveolar lavage fluid

CMV:

Cytomegalovirus

CrAg:

Cryptococcal antigen

CSF:

Cerebrospinal fluid

CT:

Computed tomography

EBV:

Epstein-Barr virus

HIV:

Human immunodeficiency virus

HPS:

Hemophagocytic syndrome

LDH:

Lactic dehydrogenase

mNGS:

Metagenomic next-generation sequencing

MRI:

Magnetic resonance imaging

PJP:

Pneumocystis jirovecii Pneumonia

SMZ:

Sulfamethoxazole

TE:

Toxoplasmic encephalitis

TMP:

Trimethoprim

References

  1. Rostami A, Riahi SM, Abdollahzadeh Sagha S, Taghipour A, Sepidarkish M, Mohammadnia-Afrouzi M, Ebrahimpour S, Hotez PJ, Gamble R, Gasser RB. Seroprevalence estimates of latent and acute Toxoplasma infections in HIV+ people-call for action in underprivileged communities. Microorganisms. 2021;9(10):2034.

    Article  Google Scholar 

  2. Gay J, Gendron N, Verney C, Joste V, Dardé ML, Loheac C, Vrtovsnik F, Argy N, Houze S. Disseminated toxoplasmosis associated with hemophagocytic syndrome after kidney transplantation: a case report and review. Transpl Infect Dis. 2019;21(5):e13154.

    Article  Google Scholar 

  3. Yang Y, Zuo W, Hu J, Esch GW, Zuo Y. Hemophagocytic syndrome as uncommon presentation of disseminated toxoplasmosis in an immunocompetent adult from Chinese Kunming. Am J Trop Med Hyg. 2013;88(6):1209–11.

    Article  Google Scholar 

  4. Telles JP, de Andrade PM, Marcusso R, Correa K, Teixeira RFA, Tobias WM. Hemophagocytic syndrome in patients living with HIV: a retrospective study. Ann Hematol. 2019;98(1):67–72.

    Article  CAS  Google Scholar 

  5. Kodym P, Machala L, Rohácová H, Sirocká B, Malý M. Evaluation of a commercial IgE ELISA in comparison with IgA and IgM ELISAs, IgG avidity assay and complement fixation for the diagnosis of acute toxoplasmosis. Clin Microbiol Infect. 2007;13(1):40–7.

    Article  CAS  Google Scholar 

  6. Camargo ME, Leser PG, Rocca A. Rheumatoid factors as a cause for false positive IgM anti-toxoplasma fluorescent tests. A technique for specific results. Rev Inst Med Trop Sao Paulo. 1972;14(5):310–3.

    CAS  PubMed  Google Scholar 

  7. Rajput R, Denniston AK, Murray PI. False negative Toxoplasma serology in an immunocompromised patient with PCR positive ocular Toxoplasmosis. Ocul Immunol Inflamm. 2018;26(8):1200–2.

    Article  Google Scholar 

  8. Blanche P, Robert F, Dupouy-Camet J, Sicard D. Toxoplasmosis-associated hemophagocytic syndrome in a patient with AIDS: diagnosis by the polymerase chain reaction. Clin Infect Dis. 1994;19(5):989–90.

    Article  CAS  Google Scholar 

  9. Guillaume M-P, Driessens N, Libert M, De Bels D, Corazza F, Karmali R. Hemophagocytic syndrome associated with extracerebral toxoplasmosis in an HIV-infected patient. Eur J Intern Med. 2006;17(7):503–4.

    Article  Google Scholar 

  10. Machala L, Malý M, Beran O, Jilich D, Kodym P. Incidence and clinical and immunological characteristics of primary Toxoplasma gondii infection in HIV-infected patients. Int J Infect Dis. 2013;17(10):e892–6.

    Article  Google Scholar 

  11. Reiter-Owona I, Bialek R, Rockstroh JK, Seitz HM. The probability of acquiring primary Toxoplasma infection in HIV-infected patients: results of an 8-year retrospective study. Infection. 1998;26:20–5.

    Article  CAS  Google Scholar 

  12. Chan E. A ‘rash’ of toxoplasmosis. Arch Intern Med. 1993;153(6):780–2.

    Article  CAS  Google Scholar 

  13. Charles PE, Doise JM, Quenot JP, Aube H, Dalle F, Bour JB, Chavanet P, Blettery B. An unusual cause of acute respiratory distress in a patient with AIDS: primary infection with Toxoplasma gondii. Scand J Infect Dis. 2003;35(11–12):901–2.

    PubMed  Google Scholar 

  14. Dong H, Ruijing Su, Yaoyao Lu, Wang M, Liu J, Jian F, Yang Y. Prevalence, risk factors, and genotypes of Toxoplasma gondii in food animals and humans (2000–2017) from China. Front Microbiol. 2018;9:2108.

    Article  Google Scholar 

  15. Shen G, Wang X, Sun H, Gao Y. Seroprevalence of Toxoplasma gondii infection among HIV/AIDS patients in eastern China. Korean J Parasitol. 2016;54(1):93–6.

    Article  Google Scholar 

  16. Rey MF, Mary C, Sanguinetti D, Ranque S, Bartoli C, L’Ollivier C. Successful treatment of pulmonary and cerebral toxoplasmosis associated with Pneumocystis pneumonia in an HIV patient. Diseases. 2017;5(4):35.

    Article  Google Scholar 

  17. Martin-Blondel G, Alvarez M, Delobel P, Uro-Coste E, Cuzin L, Cuvinciuc V, Fillaux J, Massip P, Marchou B. Toxoplasmic encephalitis IRIS in HIV-infected patients: a case series and review of the literature. J Neurol Neurosurg Psychiatry. 2011;82(6):691–3.

    Article  Google Scholar 

  18. Dinardo AR, Lewis DS, Koo HL, Goodman JC, Chiao E, Andrade R. Paradoxical immune reconstitution inflammatory syndrome due to toxoplasmic encephalitis: two cases and review of initiation of antiretroviral timing in toxoplasmic encephalitis IRIS. F1000Res. 2013;30(2):133.

    Article  Google Scholar 

  19. Zhiliang Hu, Weng X, Chunhua Xu, Lin Y, Cheng C, Wei H, Chen W. Metagenomic next-generation sequencing as a diagnostic tool for toxoplasmic encephalitis. Ann Clin Microbiol Antimicrob. 2018;17(1):45.

    Article  Google Scholar 

Download references

Acknowledgements

We thank the patient for agreeing to submit his case. We also thank the Wang Yu, Liu Sheng, Wang JinYong (Department of Infectious Diseases of the First Affiliated Hospital of China Medical University) for their professional assistance. We would like to thank Editage (www.editage.cn) for English language editing.

Funding

This work was supported by the “double first-Class” university and discipline construction funds of China Medical University (3110119068 to Ying Wen). And Ying Wen made the conception and design of the work and the fund supports patients to complete mNGS testing.

Author information

Authors and Affiliations

Authors

Contributions

YW made the conception and design of the work. YZ helped to collect the data of the case. YW, YZ, YFL wrote the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Ying Wen.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

The patient has provided written informed consent for the publication of this report.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zhou, Y., Liu, Y. & Wen, Y. Primary Toxoplasma gondii infection-associated with hemophagocytic syndrome in a man with HIV infection: a case report. BMC Infect Dis 22, 35 (2022). https://doi.org/10.1186/s12879-021-07022-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12879-021-07022-6

Keywords