Progressive Worsening of Neurological Manifestations in HIV-Associated Opportunistic Central Nervous System (CNS) Infection Patients After COVID-19 Vaccinations: A Possible Co-Incidence Causality.

BACKGROUND The iceberg phenomenon (in which the most of a problem is invisible) of people living with HIV/AIDS, particularly those with unknown HIV status, has been epidemiologically challenging. Central nervous system (CNS) opportunistic infections in patients with HIV/AIDS are one of the leading causes of morbidity and mortality in people living with HIV/AIDS. There are currently limited data on the immunogenicity, safety, and efficacy of COVID-19 vaccines in people living with HIV/AIDS with its associated opportunistic CNS infections as well as those without antiretroviral treatment. CASE REPORT Two young men with previously unknown HIV status and its related opportunistic infections received their first doses of COVID-19 vaccine (Vero Cell), inactivated. Both patients had the risk factor of having sex with men (men who have sex with men). Fever and first neurological symptoms occurred within the first few days after vaccination. Both patients were hospitalized and were tested positive for HIV for the first time. Both were further diagnosed from brain imaging as having CNS opportunistic infections. A presumptive diagnosis of cerebral toxoplasmosis was established as the working diagnosis according to the laboratory and epidemiological factors. Despite the treatment, neurological and clinical deficits worsened and eventually led to death in both patients. CONCLUSIONS The causality analyses showed that both adverse events had a possible inconsistent causal relationship to COVID-19 vaccination. Our cases may reflect the need for further studies on the safety of COVID-19 vaccines in people with HIV/AIDS-associated CNS opportunistic infection as well as people with HIV/AIDS who never receive antiretroviral treatment (ART).

Background

CNS opportunistic infections in patients with HIV/AIDS are one of the leading causes of morbidity and mortality in PLWHA, despite the introduction to ART [1-3]. Some agents causing central nervous system (CNS) opportunistic infections, such as Toxoplasma gondii, Cytomegalovirus, and Cryptococcus, resulting in cerebral toxoplasmosis, cytomegalovirus encephalitis, and cryptococcal meningitis, could indicate the immunocompromised status of PLWHA, since they mostly infect PLWHA with CD4+ count less than 200 cells/mm3 [1,2]. Despite the overall low incidence of HIV-associated CNS infections, all PLWHA with advanced HIV infection should be suspected to have a CNS opportunistic infection [1]. However, people with unknown HIV status but who have risk factors for HIV infection may also present with the symptoms of CNS opportunistic infections as the first clinical manifestations [1]. In HIV-associated CNS infections, temporal evolution from symptom onset to presentations ranges from days to weeks and after appropriate treatments, months-to-years survival can also be observed [1].

The COVID-19 pandemic has been declared since March 2020 by the WHO until recently. Development and distribution of vaccines against SARS-COV-2 have been accelerated to end the pandemic era to protect healthcare systems, restore the global economy, and reinstate normal social interactions. PLWHA, at any stage of the disease, are recommended by the WHO and CDC as priority targeted subjects for COVID-19 vaccination [4]. The data on efficacy and safety of COVID-19 vaccine in PLWHA are still limited to those with stable HIV stage who have been receiving ART. Two studies reported that the COVID-19 vaccine ChAdOx1 nCoV-19 was safe and immunogenic in PLWHA with ART and CD4+ count >350 cells/µl [5,6]. Other studies reported that inactivated COVID-19 vaccine showed safety in PLWHA who received ART but a poor immunological response was observed in those with CD4+ count <350 cells/µl [7]. Furthermore, there are also no data reporting that these COVID-19 vaccines are inefficacious and unsafe or interfere with ART [5-8]. Here, we report 2 cases of young men with previously unknown HIV status whose neurological symptoms emerged and worsened progressively after receiving the first dose of vaccine against SARS-CoV-2.

Case Reports

Patient 1

A 23-year-old single man was brought to the ED with acute onset of high fever and weakness in his left arm and leg. The fever had persisted for the last 10 days despite taking over-the-counter paracetamol. He felt weakness in his left leg and arm for the last 5 days. He reported that he felt low-intensity headaches once or twice a week in the last few months. The headache was relieved with rest and over-the-counter paracetamol.

The patient received the first dose of COVID-19 vaccine (Vero Cell, inactivated) 2 days before the fever started. A marked body weight reduction and history of having sex with men (men who have sex with men – MSM) were reported. He said he had been healthy prior to the present illness.

The patient presented with general weakness, body temperature of 38.5°C, and fully conscious. On neurologic examination, upper motor neuron type of left facial nerve weakness was found. His left arm and leg could only move against gravity, without any activity against the examiner’s low resistance. Increased physiological reflexes, pathological reflexes, and clonus were found in his left extremities. Neck stiffness and Kernig sign were also found.

On laboratory examination, normal white blood cell (WBC) count with low lymphocyte count and low presumptive CD4+ count of 154 were found (). Critical serum hyponatremia was also found. He tested reactive and positive for HIV-rapid and ELISA HIV, respectively. TORCH examination showed increased serum IgG levels of anti-toxoplasma, anti-CMV, and anti-rubella, with high avidity on both anti-toxoplasma and anti-CMV IgG. A chest X-ray showed suspected signs of atypical pneumonia in his right lung (). He was scheduled for brain imaging and lumbar puncture, but he refused the lumbar puncture procedure.

He was presumptively diagnosed with cerebral toxoplasmosis and was treated with oral pyrimethamine. Intravenous dexamethasone and CNS-dosing ceftriaxone were given as empirical therapy for possible bacterial meningoencephalitis. Intravenous paracetamol was given as an antipyretic for fever. His serum sodium level was corrected with intravenous hypertonic saline. On the third day of inpatient care, the patient decided to be discharged from the hospital.

Three days after hospital discharge, the patient was brought again to the ED due to seizures and decreased consciousness. His family witnessed general tonic clonic seizure 3 times, with duration of 2–3 min each in the last 12 h. His fever, left extremity weakness, and headache persisted.

On this second admission, he had body temperature of 39.2°C, GCS of E3V2M5, heart rate 111 beats per minute, and respiration rate 22 times per minute. The left facial nerve weakness, left extremity weakness, neck stiffness, Kernig sign, increased physiological reflexes, pathological reflexes, and clonus findings were consistent with his first admission.

On laboratory examination, a normal WBC with low lymphocyte count and low presumptive CD4+ count of 174, serum hyponatremia, and hypercoagulation were found. Urinalysis showed marked bacteriuria and leukocyturia but the history of urinary tract symptoms was unknown. His chest X-ray showed right para-hilar infiltrates, suggesting pneumonia from tuber-culous infection (). A contrast head CT scan showed multiple foci in bilateral frontal and parietal lobes with perifocal edema with midline shift to the left (). According to these examinations, our working diagnosis for this patient was cerebral toxoplasmosis with a differential diagnosis of tuberculous meningoencephalitis, as well as pulmonal tuberculosis in an HIV/AIDS patient. The chronological timeline of the patient’s disease course is presented in .

The presumptive cerebral toxoplasmosis was treated with oral pyrimethamine and cotrimoxazole. Intravenous dexamethasone and Ceftazidime were given as empirical therapy for possible bacterial meningoencephalitis. A fixed-dose antituberculosis drug combination containing rifampicin, isoniazid, pyrazin-amide, and ethambutol was given for the pulmonary tuberculosis as well as the possible tuberculous meningoencephalitis.

The seizure was treated with intravenous phenytoin and intravenous paracetamol was given as an antipyretic for fever. Serum hyponatremia was corrected using hypertonic saline. On daily evaluation, his consciousness improved to somnolence and his general tonic seizure did not re-occur. However, continuous focal myoclonus of the right arm was observed. Intravenous phenytoin was then switched into oral valproic acid. His focal myoclonus stopped 1 day following the first administration of valproic acid. Unfortunately, his condition worsened on the third day of his second hospitalization. Sepsis was confirmed from his clinical and laboratory findings. He eventually developed acute respiratory distress syndrome and septic shock, which led to death.

Patient 2

A 23-year-old single man was brought to the ED with altered mental status preceded by acute exacerbating headache and fever. His family stated that he was just discharged from another hospital 3 days before his current admission, due to fever, headache, and 2 separate events of general tonic clonic seizure. Non-contrast head CT scan from his first inpatient care showed no abnormality. In addition, he tested reactive on the HIV-rapid test. He had been free from fever, headache, and seizure after his first inpatient care in the previous hospital before the symptoms occurred again and worsened 1 day before his current admission.

His family said that he had a history of MSM and reported significant weight loss. He was also reported to have no symptoms of any disease as far as his family recalled. The patient received his first dose of COVID-19 vaccine (Vero Cell, inactivated) 14 days before current hospital admission.

On his current admission, he had GCS of E4V4M5 and body temperature of 38.6°C with normal blood pressure, respiration rate, and heart rate. A neurological examination showed neck stiffness and Kernig sign with normal cranial nerve examinations and no lateralization. The motoric examination, physiological reflexes, and pathological reflexes were normal. Laboratory examination showed normal WBC with normal lymphocyte count and estimated CD4+ count of 382. Serum hypercoagulation was found, with D-dimer count of 1785 µg/ml. He tested positive for ELISA HIV, TPHA, and VDRL. TORCH examination showed elevated serum IgG levels of anti-toxo-plasma, anti-CMV, and anti-rubella, with high avidity on both anti-toxoplasma and anti-CMV IgG (). A blood culture grew no bacteria or fungi.

Lumbar puncture was performed on the day after his admission, and his CSF analysis showed pleocytosis (127 mononuclear cells and 3 polymorphonuclear cells/µl), elevated protein (0.14 gr/dl), and decreased CSF/serum glucose ratio (38%). Immunochromatographic testing for Cryptococcus and rapid molecular test for tuberculosis showed negative results.

A chest X-ray showed para-hilar and para-cardiac infiltrates in his left lung (). A contrast brain MRI showed multiple lesions in both cerebral and cerebellar hemispheres, suggesting cerebral toxoplasmosis (). He was diagnosed with presumptive cerebral toxoplasmosis and atypical community-acquired pneumonia in an HIV/AIDS patient. The chronological timeline of the patient’s disease course is shown in .

He was given oral pyrimethamine to treat the presumptive cerebral toxoplasmosis. Intravenous dexamethasone and CNS-dosing ceftriaxone were given as empirical therapy for possible bacterial meningoencephalitis. The atypical community-acquired pneumonia was treated with oral azithromycin. Oral phenytoin and paracetamol were given as antiepileptic and antipyretic drugs, respectively. On the fifth day of inpatient care, he developed progressive decrease of consciousness, worsening headache, frequent vomiting, and seizures, suggesting elevated intracranial pressure, which led to death.

Discussion

Epidemiologically, our national and global society has been facing the iceberg phenomenon of PLWHA, particularly those whose HIV status is not known, as in 2 patients reported here [9,10]. There were 37.6 million PLWHA across the globe in 2020, and 95.5% of them were adults. In the same year, the global HIV incidence was 1.5 million individuals [9]. This estimated HIV incidence number includes individuals who might have acquired HIV infection without knowing it. In Indonesia, the estimated number of PLWHAs in 2020 was 543 100, with 32 293 new cases, and a total of 409 857 people living with HIV/AIDS were reported in the annual HIV/AIDS report from the Ministry of Health of the Republic of Indonesia [10]. HIV status may be crucial in the current COVID-19 era due to the growing evidence that suggest PLWHA as an independent risk factor for higher morbidity and mortality in COVID-19 outcomes [4,11]. The increased risk of morbidity and mortality due to COVID-19 in PLWHA was also reported despite the successful HIV treatment, suggesting immune deficiency as the culprit [12]. Therefore, there are national and international consensuses regarding the necessity of COVID-19 vaccinations in PLWHA, despite the limited data on the efficacy and safety of the vaccines in these subpopulations [13]. In some countries, including Indonesia, it is necessary for people with certain medical conditions, including PLWHA whose HIV infection status has been known, to have a physician’s recommendation for COVID-19 vaccination in spite of the safety claim from the WHO and CDC for COVID-19 vaccinations in PLWHA [4,14].

We performed causality analyses on the adverse events following immunization in these 2 patients (). The results showed that both adverse events had an inconsistent causal relationship with immunization [15]. Therefore, these cases were both coincidental events following COVID-19 vaccinations in patients with unknown medical conditions that turned out to be PLWHA with CNS opportunistic infections. The occurrence of CNS opportunistic infections was not only caused by the noncompliance with ART and ART’s resistance in HIV patients with ART, but also the unawareness of the HIV-positive status in some individuals [2]. Furthermore, these HIV-related CNS opportunistic infections can cause major morbidity and mortality in HIV patients despite the ART, since these opportunistic infections may reflect the low CD4+ count as well as the severe degree of HIV infections, particularly in low-to-middle income countries [2,16]. Diagnosis evaluation in HIV-related CNS opportunistic infections should be based on local neuroepidemiology, the degree of immunosuppression, and individual clinical, laboratory, and brain imaging features throughout the disease course [16].

There are currently limited data on the immunogenicity of COVID-19 vaccines in PLWHA, although evidence shows the importance of CD4+ and CD8+ T cells in the immunologic memory component in the host response to SARS-COV-2 infection [17,18]. Previous studies suggested that immune response in recombinant hepatitis B vaccination in PLWHA whose CD4+ lymphocytes are <50/mm3 was not effective [19]. Furthermore, shorter duration of seroprotection in PLWHA was confirmed after vaccinations against hepatitis B, hepatitis A, measles, mumps, and rubella, tetanus, poliomyelitis, and pertussis, and some other pathogens [20]. Immunization while PLWHA are on ART, as well as increasing the antigen dose, are known as 2 strategies for improving the long-term seroprotection in vacci-nation in this subpopulation [20]. Unfortunately, neither strategy was applied in our patients due to their unknown HIV status.

Our current knowledge on COVID-19 vaccination in PLWHA was based on the findings from trials involving stable HIV patients that suggest the safety, tolerability, and immunogenicity of COVID-19 vaccines [5-8]. This is also emphasized by the recommendations of the WHO and CDC for COVID-19 vacci-nation in PLWHA [4]. To date, there is no clear understanding of adverse events following COVID-19 vaccination in PLWHA with previously unknown HIV status. The closest study we found to our current report was a case report in a treatment-naïve HIV-positive patient who experienced deterioration of HIV infection after receiving the first dose of an inactivated COVID-19 vaccine [21]. This report suggested the possibility of activated HIV infection that directly increased the rate of CD4+ T cells destruction, thus causing serial depletion of CD4+ T cells. This report also suggested that ART initiation in the case of treatment-naïve PLWHA could be beneficial to preserve immune function, prevent secondary HIV transmission, and prevent complications of health conditions or procedures, including vaccines [21]. In addition, infection with HIV-1 and SARS-CoV-2 causes marked CD4+ T cell lymphopenia by the mechanisms of direct CD4+ T cells attacks, immune activation, and CD4+ T cell redistributions [22]. As for COVID-19 vaccination, proper CD4+ T cell function is necessary for an effective vaccine response [22].

In our present cases, both patients were diagnosed with CNS opportunistic infections at the same time as their confirmed HIV infection. At this point, the CNS opportunistic infections in these patients may have reflected the advanced HIV infection [1], despite the presumptive CD4+ count in our reported cases. In other words, the presumptive cerebral toxoplasmosis found in both patients was an AIDS-defining illness regardless of CD4+ count. Based on the previously reported case, we speculate that possible activation of HIV infection after inactivated COVID-19 vaccine injection led to increased CD4+ T cells destruction, which in turn caused progressive clinical deteriorations in the reported cases [21]. However, it should be taken into account that this speculation is based on only a single case report of a treatment-naïve HIV-positive patient and the findings cannot be generalized to other patients with HIV. It is important to follow the COVID-19 vaccination guidelines according to the regional or national regulations, particularly for those with comorbidities. The Indonesian Society of Internal Medicine recommended that COVID-19 vaccination for PLWHA can be performed if their condition is stable and they are receiving routine ART [23].

There are limitations of our study: (i) CNS opportunistic infections were established according to the presumptive diagnosis criteria of cerebral toxoplasmosis and its differential diagnosis, (ii) CD4+ count was performed using presumptive CD4 count, and whether it reflects the true CD4+ count is unclear, and (iii) there is limited evidence of vaccination error. There is a need for further studies on the safety of COVID-19 vaccines in PLWHA without ART as well as HIV/AIDS-associated CNS opportunistic infections. The early initiation of ART after COVID-19 vaccination was previously reported to be beneficial in treatment-naïve PLWHA, but this can only be performed if the HIV status is determined.

Conclusions

Here, we presented 2 cases that were possible coincidental events between treatment-naïve PLWHA with CNS opportunistic infections after COVID-19 vaccinations. Our cases may extend the needs for further studies on the safety of COVID-19 vaccines in HIV/AIDS-associated CNS opportunistic infection as well as HIV/AIDS patients who never received antiretroviral treatment (ART).

Patient 1

Step 1. Background.

Data availability: Yes

Does the diagnosis meet the case definition? Yes

Vaccine type: inactivated COVID-19 vaccine

Step 2. Questions of Adverse Events Following Immunization.

I. Is there strong evidence of other causes?
Is clinical or laboratory tests in this patient confirming other causes?	Yes
II. Is there any known causal relationship with the vaccination?
Vaccine products
Is there any previous evidence that the vaccine may cause Adverse Events Following Immunization even if it is appropriately given?	No
Is there a specific test showing the causal role of the vaccine or its composition?	No
Immunization error
Was there any error in prescribing or of the vaccine’s recommendation use? (Example: expired date, inappropriate recipient, etc)	N/A
Was the vaccine (or its composition) given in sterile procedure?	N/A
Was there any abnormality in the vaccine’s physical condition (example: color change, increased turbidity, foreign material, etc) during immunization?	N/A
Was there any error on the vaccine’s preparation (example: inappropriate product, inappropriate diluent, inappropriate syringe preparation, etc)?	N/A
Was there any error in the vaccine’s handling (example: cold chain failure on delivery, storage, or immunization)?	N/A
Was the vaccine given inappropriately? (example: inappropriate dose, inappropriate application, inappropriate syringe, etc)	N/A
Immunization anxiety
Can the adverse events following immunization be caused by anxiety due to immunization? (example: vasovagal reflex, hyperventilation, or stress)	No
Did the adverse event occur within time window after immunization?	Yes
III. Is there any strong evidence to deny the causal relationship?
Is there any strong evidence to deny the causality relationship?	No
IV. Other qualification factors for classification
Can the adverse event occur independently without vaccination (background rate)?	Yes
Can the adverse event occur as a manifestation from other health condition?	Yes
Does the adverse event occur after a similar vaccine’s dose as previously given?	No
Was there any exposure to other toxins or potential risk factors?	Yes
Was there any acute disease before the adverse event occurs?	No
Was there any previous adverse event that did not relate to the vaccine?	No
Did the patient use any medications before the adverse events occurs?	No
Are there any logic biological causes explaining the vaccine with the adverse events?	Yes

Patient 2

Step 1. Background.

Data availability: Yes

Does the diagnosis meet the case definition? Yes

Step 2. Questions of Adverse Events Following Immunization.

I. Is there strong evidence of other causes?
Do clinical or laboratory tests in this patient confirm other causes?	Yes
II. Is there any known causal relationship with the vaccination?
Vaccine products
Is there any previous evidence that the vaccine may cause adverse events? Following Immunization even if it is appropriately given?	No
Is there a specific test showing the causal role of the vaccine or its composition?	No
Immunization error
Was there any error in prescribing or of the vaccine’s recommendation use? (Example: expired date, inappropriate recipient, etc)	N/A
Was the vaccine (or its composition) given in sterile procedure?	N/A
Was there any abnormality in the vaccine’s physical condition (example: color change, increased turbidity, foreign material, etc) during immunization?	N/A
Was there any error on the vaccine’s preparation (example: inappropriate product, inappropriate diluent, inappropriate syringe preparation, etc)?	N/A
Was there any error in the vaccine’s handling (example: cold chain failure on delivery, storage, or immunization)?	N/A
Was the vaccine given inappropriately? (example: inappropriate dose, inappropriate application, inappropriate syringe, etc)	N/A
Immunization anxiety
Can the adverse events following immunization be caused by anxiety due to immunization? (example: vasovagal reflex, hyperventilation, or stress)	No
Did the adverse event occur within the time window after immunization?	Yes
III. Is there any strong evidence to deny the causal relationship?
Is there any strong evidence to deny the causal relationship?	No
IV. Other qualification factors for classification
Can the adverse event occur independently without vaccination (background rate)?	Yes
Can the adverse event occur as a manifestation from other health condition?	Yes
Did the adverse event occur after a similar vaccine’s dose as previously given?	No
Was there any exposure to other toxins or potential risk factors?	Yes
Was there any acute disease before the adverse event occurred?	No
Was there any previous adverse event that was not related to the vaccine?	No
Did the patient use any medications before the adverse events occurred?	No
Are there any logic biological causes explaining the vaccine adverse events?	Yes

Table 1.

Patients’ clinical, laboratory, and imaging findings.

Parameters	Patient 1	Patient 2	Normal range
COVID-19 vaccine type	Inactivated vaccine	Inactivated vaccine
Clinical manifestations
Onset from COVID-19 vaccine	2 days	2 weeks
General examinations	Temperature: 38.5°CBlood pressure: 147/91 mmHgPulse rate: 104 bpmRespiratory rate: 22 times per minute	Temperature: 38.6°CBlood pressure: 132/83 mmHgPulse rate: 86 bpmRespiratory rate: 20 times per minute
Neurological deficits on first admission	GCS E4V5M6SeizureNoneCranial nerves:paralysis of left CN. VII upper motor neuron typeMotoric:left hemiparesis with strength score 3Physiological reflexes:+3 in left upper extremity+4 in left lower extremityPathological reflexes:Hoffman reflex (+) and Tromner reflex (+) in left upper extremityBabinski great toe reflex (+) in left lower extremityClonus:(+) in left lower extremityMeningeal signs:(+) for neck stiffness and Kernig sign	GCS E4V5M6Seizure:General tonic clonic seizure, repeatedCranial nerves:No dataMotoric:No dataPhysiological reflexes:No dataPathological reflexes:No dataClonus:No dataMeningeal signs:No data
Neurological deficits on second admission	GCS E2V3M5Seizure:General tonic clonic seizure, repeatedCranial nerves:paralysis of left CN. VII upper motor neuron typeMotoric:left hemiparesis with strength score 3Physiological reflexes:+3 in left upper extremity+4 in left lower extremityPathological reflexes:Hoffman reflex (+) and Tromner reflex (+) in left upper extremityBabinski great toe reflex (+) in left lower extremityClonus:(+) in left lower extremityMeningeal signs:(+) for neck stiffness and Kernig sign	GCS E4V4M5Seizure:General tonic clonic seizureCranial nerves:No abnormalityMotoric:No lateralizationPhysiological reflexes:+2 in all extremitiesPathological reflexes:NoneClonus:NoneMeningeal signs:None
Risk factors for HIV infection	Men who have sex with men (MSM)	Men who have sex with men (MSM)
Summary of laboratory findings
WBC (103/µL)	8.05	6.21	4.50–11.50
Neutrophil (%)	78.6	57.1	50–70
Lymphocyte (%)	9.6	30.8	18–42
Monocyte (%)	11.7	11.7	2–11
Basophil (%)	0.1	0.2	0–2
Eosinophil (%)	0.0	0.2	1–3
Presumptive CD4 count	154	382	> =200
Hemoglobin (g/dL)	13.7	11.0	13.0–18.0
Albumin (g/dL)	3.79	3.34	3.40–5.00
C-reactive protein (mg/L)	7	38	<5
Sodium (mmol/L)	123	135	136–145
Potassium (mmol/L)	3.98	3.70	3.50–5.10
Chloride (mmol/L)	87	98	98–107
D-dimer (ng/mL)	640	1785	<250
Urinalysis
Glucose	Negative	Negative	Negative
Protein	1+	+−	Negative
Blood	3+	1+	Negative
Leucocyte esterase	2+	Negative	Negative
Bacteria (/µL)	844.5	4.8	0–100
IgM Anti-Toxoplasma	0.06	0.01	Negative: <0.55Equivocal: 0.55–0.64Positive: ≥0.65
IgG Anti-Toxoplasma (IU/mL)	273	437.0	Negative: <4Equivocal: 4–7Positive: ≥8
Avidity Toxoplasma	0.522	0.64	Weak: <0.20Moderate: ≥0.20–0.29Strong: ≥0.30
IgM Anti-rubella	0.08	0.10	Negative: <0.80Equivocal: 0.80–1.19Positive: ≥1.20
IgG Anti-rubella (IU/mL)	26.0	187.0	Negative: <10.00Equivocal: 10.00–14.00Positive: ≥15.00
IgM Anti-CMV	0.02	0.14	Negative: <0.70Equivocal: 0.70–0.89Positive ≥0.90
IgG Anti-CMV (AU/mL)	34.00	51.00	Negative: <4.00Equivocal: 4.00–5.00Positive: ≥6.00
Avidity CMV	0.907	0.90	Weak: <0.4Moderate: 0.4–0.64Strong: ≥0.65
IgM Anti-HSV1 (U/mL)	0.3	1.8	Negative: <20.0Borderline: 20.0–25.0Positive: >25.0
Blood Gas Analysis
pH	7.411	7.63	7.35–7.45
pCO2	43.4	23.1	35.0–45.0
HCO3	27.2	24.5	22.0–26.0
pO2	62	122.6	80.0–95.0
sO2%	90	98.2	96.0–97.0
pO2/FiO2		524.6
BE	3	3.8
BEb		5.6
A		112.4
a/A		1.1
CSF Analysis	N/A	Pleocytosis (130 cells/µL)Elevated Protein (0.14 gr/dL)Decrease CSF/Serum GlucoseRatio (38%)Cryptococcus ICT: NegativeMTB Rapid Molecular Test:Negative
Brain imaging	Contrast Head CT scan: Multiple foci in bilateral frontal and right parietal with perifocal edema, causing midline shift to the left	Non-contrast head CT scan: normalContrast brain MRI: multiple foci in bilateral cerebral and cerebellar with perifocal edema
Other opportunistic infections	Pulmonary tuberculosis	Lung pneumonia, unspecified