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AIDS CLINICAL ROUNDS
The UC San Diego AntiViral Research Center sponsors weekly
presentations by infectious disease clinicians, physicians and
researchers. The goal of these presentations is to provide the most
current research, clinical practices and trends in HIV, HBV, HCV, TB
and other infectious diseases of global significance.

The slides from the AIDS Clinical Rounds presentation that you are
about to view are intended for the educational purposes of our
audience. They may not be used for other purposes without the
presenter’s express permission.
Toxoplasmosis, malaria, and HIV:
Impact of latent co-infection on HIV
              disease
           Ajay R. Bharti, MD
           Assistant Professor
     Division of Infectious Diseases

                                       1
Toxoplasmosis
• Toxoplasma gondii
• Acute infection
   – Flu-like symptoms that resolve in a few weeks
   – CMI controls but does not eradicate the parasite
   – May cause congenital infection
• Latent infection
   – Life long
   – Dormant in tissue
      • Brain: neurons and astrocytes
      • Muscle: skeletal, heart, and smooth muscle
   – Reactivation disease after loss of CMI
   – Encephalitis and chorioretinitis

                                                        2
T. gondii Life Cycle




                       3
Epidemiology




               4
LT Prevalence in USA




                       5
Increasing Prevalence with Age




                                 6
7
LT Prevalence in France




                          8
9
LT and HIV Co-infection




                          10
Toxoplasma seroprevalence among HIV-infected
patients
•   Mathews, WC and Fullerton, SC
•   July 1, 1986 to March 31, 1990
•   Laboratory database of 1599 HIV+ patients
•   344 had Toxo IgG results
•   LT seroprevalence of 16%




                          Arch Pathol Lab Med. 1994 Aug;118(8):807-10.   11
LT seroprevalence among HIV+ population in southern Alberta,
                         Canada




                                                           12
•   St. Paul hospital, Addis Ababa
•   Tested 330 samples (165 HIV+, 165 HIV-)
•   Overall seroprevalence 90%
•   High but similar in both groups
    – HIV+ (93.3%) vs. HIV- (86.7%)




                                              13
A=31%
B=68%
C=28%




        14
  JPM, 1997
•   Prospective study
•   Recruited 79 subjects
•   LT seroprevalence similar in HIV+ and HIV-
•   Overall prevalence of 64%




                                                 15
Impact of LT on Brain




                        16
Animal Studies




                 17
18
19
Morris water maze
Human Studies




                20
• Case control study
  – 54 suicide attempters and 30 controls
• Self-directed violence assessed by SUAS-S
  score




                                       J Clin Psy, Aug 2012
                                                          21
• Violent suicide attempts, RR=1.81 (95% CI, 1.13-2.84)
• Suicide, RR=2.05 (95% CI, 0.78-5.20)

                                                          22
• First study to investigate the effect of LT in
  humans
• Significant delay in reaction time in those with
  LT
• Positive correlation between length of
  infection and mean reaction time



                                                 23
24
• Prospective study of 3,890 male subjects
• LT increased the chance of traffic accidents
  – (OR 2.43, CI95: 1.11–5.35, P = 0.027)
• RhD positivity reduced the risk of traffic
  accidents in LT+ subjects
  – (OR 0.35, CI95: 0.136–0.902, P= 0.028)
• RhD+ people are protected against LT-induced
  impaired reaction time
                                                 25
• 758 women in 16th
  week of gestation
• LT+ women had a
  lower body weight
  (p = 0.02)
• Cumulative effect



                      26
Other Effects of LTI
•   Alzheimer’s disease
•   Parkinson’s disease
•   Schizophrenia
•   OCD
•   Increases probability of birth of male offspring
•   Effect on personality
    – High intelligence, guilt proneness, radicalism, and
      high ergic tension
                                                            27
28
Mechanism behind impact of LT on
            brain




                                   29
TH within cysts




                     30
PC12 cell culture
• Cysts widely distributed in brain
• Cerebral cortex had higher cyst density than
  subcortical region
• Cerebellum consistently had low cysts
• Myelinated fiber tracts devoid of cysts
• No tropism towards dopaminergic or
  hypothalamic systems

                                                 31
• Men with LT had decreased leukocyte, NK-cell
  and monocyte counts
• Women had increased counts
• B-cell counts were reduced in both men and
  women
• The difference between LT+ and LT- subjects
  declined with decline in Toxo IgG titers


                                             32
Our Findings




               33
Background
• Prevalence of LT is similar or higher in HIV+
  compared with HIV- individuals
• ARVs do not affect LT
• HIV-associated neurocognitive disorders
  persist despite adequate ART
  – Co-infections like LT may contribute to NCI
• Impact of LT on neurocognitive impairment in
  HIV+ individuals has not been studied

                                                  34
Objectives
• To determine the prevalence of LT in our HIV+
  cohort
• To evaluate its impact on neurocognitive
  functioning




                                                  35
Methods
• Randomly selected 120 HIV+ participants from an NIH-
  funded cohort project
• Toxoplasma IgG was measured in serum by commercial
  immunoassay
• HNRC neurocognitive test battery was used
   – Tests 7 ability areas
• Performance was summarized as the validated global
  deficit score (GDS)
   – GDS ≥ 0.5 defined neurocognitive impairment
• Data were analyzed by routine statistical methods,
  including Pearson’s correlations and linear regression

                                                           36
Neuropsychological Test Battery

Verbal Fluency              Executive Functioning
   Sound                       Category Test
   Animals                     WCST-64
   Action                      Color Trails II
Attn/Working Memory         Learning/Memory
   PASAT-50                    Verbal (Hopkins Verbal Learning
   WMS-III Spatial Span           Test - Revised)
Processing Speed               Visual (Brief Visuospatial
                                  Memory Test - Revised)
   WAIS-III Digit Symbol
   WAIS-III Symbol Search
                            Motor
   Trails A                    Grooved Pegboard
   Color Trails 1
                                                            37
Results
• LT was detected in 12 (10%) participants
• LT+ subjects were similar to LT- subjects
  except that they were significantly older
• LT+ subjects were more likely to have
  neurocognitive impairment (although not
  statistically significant)
  – This difference was greater among subjects who
    were older than the median age of 44 years (60%
    vs. 33%, p = 0.11)

                                                      38
39
Results
• LT was detected in 12 (10%) participants
• LT+ subjects were similar to LT- subjects except that they
  were significantly older
• LT+ subjects were more likely to have neurocognitive
  impairment (although not statistically significant)
   – This difference was greater among subjects who were older
     than the median age of 44 years (60% vs. 33%, p = 0.11)
• Among LT+ subjects, higher IgG titers titers were
  associated with
   –   higher CD4+ T-cell counts (r=0.74, p=0.05, Fig. 1)
   –   worse GDS (r=0.31, p=0.33, Fig. 2)
   –   On excluding the 2 outliers, worse GDS (r=0.88, p=0.0007, Fig. 2)
   –   Higher memory deficit (p=0.01)

                                                                      40
Toxo titers and CD4+ count




                             41
Results
• LT was detected in 12 (10%) participants
• LT+ subjects were similar to LT- subjects except that they
  were significantly older
• LT+ subjects were more likely to have neurocognitive
  impairment (although not statistically significant)
   – This difference was greater among subjects who were older
     than the median age of 44 years (60% vs. 33%, p = 0.11)
• Among LT+ subjects, higher IgG titers titers were
  associated with
   –   higher CD4+ T-cell counts (r=0.74, p=0.05, Fig. 1)
   –   worse GDS (r=0.31, p=0.33, Fig. 2)
   –   On excluding the 2 outliers, worse GDS (r=0.88, p=0.0007, Fig. 2)
   –   Higher memory deficit (p=0.01)

                                                                      42
Toxo Titers and GDS




                      43
Results
• LT was detected in 12 (10%) participants
• LT+ subjects were similar to LT- subjects except that they
  were significantly older
• LT+ subjects were more likely to have neurocognitive
  impairment (although not statistically significant)
   – This difference was greater among subjects who were older
     than the median age of 44 years (60% vs. 33%, p = 0.11)
• Among LT+ subjects, higher IgG titers titers were
  associated with
   –   higher CD4+ T-cell counts (r=0.74, p=0.05, Fig. 1)
   –   worse GDS (r=0.31, p=0.33, Fig. 2)
   –   On excluding the 2 outliers, worse GDS (r=0.88, p=0.0007, Fig. 2)
   –   Higher memory deficit (p=0.01)

                                                                      44
Conclusions
• Prevalence of LT in our HIV+ cohort was 10%
  – Similar to the general population (10.8%)
  – Not generalizable as our cohort consisted of drug
    abusers
• LT+ older subjects trended towards worse
  neurocognitive functioning and higher anti-Toxo
  IgG titers were associated with worse functioning
• Studies with a larger number of LT+ individuals
  are needed to validate this finding

                                                        45
Future Directions
• Identify a larger HIV and LT co-infected cohort
  – Owen clinic and HNRC
• Investigate the impact on driving in more
  detail
  – Driving simulator studies
• Mechanistic studies
  – Role of inflammation: plasma and CSF
  – In vitro brain model

                                                46
Malaria




          47
Malaria
• Mosquito-borne infectious disease
• Plasmodium spp.
  – P. falciparum, P. vivax
  – P. ovale, P. malariae
• 300-500 million episodes of acute illness
• > 1 million deaths/year worldwide



                                              48
Life Cycle




             49
Malaria and HIV Interactions

•   HIV+ patients are twice as likely to get malaria*
•   ↑HIV RNA and ↓CD4 counts
•   Malaria doubles HIV-1-RNA with 0.25 log ↑**
•   HIV RNA ↑ (0.82 log ↑) greatest when
      • Febrile patient
      • Parasite density >2,000/µL
      • CD4 >300/µL
• Mathematical model
      • Village of ~200,000 had excess 8,500 HIV infections and
        980,000 malaria episodes***

*Patnaik et al J Infect Dis 2005; **Kublin et al Lancet 2005; ***Kublin Science 2006
                                                                                       50
51
Asymptomatic Malaria
• Seen in areas of high transmission
• Also reported in low edemicity regions
• Clinical immunity that controls parasitemia but does
  not completely eliminate it
• Described for both P. falciparum & P. vivax malaria
• Few studies on HIV and asymptomatic malaria co-
  infections
• Since malaria prevalence is not homogenous, sites
  need to be tested individually

                                                         52
Our Findings




               53
Study Objective
• To retrospectively determine the prevalence
  of malaria co-infection in a cohort of HIV-
  infected individuals in southern India




                                                54
Methods
• Individuals presenting to YRG CARE, Chennai,
  India between Jan 1, 2008 and Dec 31, 2008
• Stored serum samples randomly selected from
  HIV+ individuals
• Retrospectively diagnosed malaria by antibody
  testing and PCR



                                              55
Results
• Malaria co-infection
  rate 9.8% (45/460)
• PCR negative




                                   56
Discussion
• Considerable burden of malaria co-infection
• Predominently due to P. vivax
• Rate of P. falciparum 6-fold higher than in the
  general population
• Co-infected subjects not more likely to be
  immunosupressed than HIV mono-infected
• Negative PCR
   – Possibly due to parasitemia below detection limit
   – Parasite DNA degradation unlikely
• Our strategy may be used for identifying co-
  infections in areas with unstable malaria
  transmission
                                                         57
Future Directions
• Alternate site with high malaria prevalence
  – Nigeria
• Use of more suitable specimens
  – Whole blood or Dried blood spots




                                                58
59
Acknowledgements
• United States          • India
   –   Scott Letendre       – N. Kumarasamy
   –   Davey Smith          – Jabin
   –   Tom Marcotte
   –   Ron Ellis         • Nigeria
   –   Connie Benson        – Kanayo Okwuasaba
   –   Chip Schooley        – Ndidi Agala
   –   Igor Grant
   –   Allen McCutchan
                         • Funding
   – Cris Achim             – NIMH 1 K23 MH085512-01A2
   – D. J. Perkins          – CFAR International Pilot Project Grant
   – Walter Royal
                         • Study participants

                                                                       60
Questions?



             61

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Toxoplasmosis, Malaria, and HIV: Impact of Latent Co-infection on HIV Disease

  • 1. AIDS CLINICAL ROUNDS The UC San Diego AntiViral Research Center sponsors weekly presentations by infectious disease clinicians, physicians and researchers. The goal of these presentations is to provide the most current research, clinical practices and trends in HIV, HBV, HCV, TB and other infectious diseases of global significance. The slides from the AIDS Clinical Rounds presentation that you are about to view are intended for the educational purposes of our audience. They may not be used for other purposes without the presenter’s express permission.
  • 2. Toxoplasmosis, malaria, and HIV: Impact of latent co-infection on HIV disease Ajay R. Bharti, MD Assistant Professor Division of Infectious Diseases 1
  • 3. Toxoplasmosis • Toxoplasma gondii • Acute infection – Flu-like symptoms that resolve in a few weeks – CMI controls but does not eradicate the parasite – May cause congenital infection • Latent infection – Life long – Dormant in tissue • Brain: neurons and astrocytes • Muscle: skeletal, heart, and smooth muscle – Reactivation disease after loss of CMI – Encephalitis and chorioretinitis 2
  • 4. T. gondii Life Cycle 3
  • 8. 7
  • 9. LT Prevalence in France 8
  • 10. 9
  • 11. LT and HIV Co-infection 10
  • 12. Toxoplasma seroprevalence among HIV-infected patients • Mathews, WC and Fullerton, SC • July 1, 1986 to March 31, 1990 • Laboratory database of 1599 HIV+ patients • 344 had Toxo IgG results • LT seroprevalence of 16% Arch Pathol Lab Med. 1994 Aug;118(8):807-10. 11
  • 13. LT seroprevalence among HIV+ population in southern Alberta, Canada 12
  • 14. St. Paul hospital, Addis Ababa • Tested 330 samples (165 HIV+, 165 HIV-) • Overall seroprevalence 90% • High but similar in both groups – HIV+ (93.3%) vs. HIV- (86.7%) 13
  • 15. A=31% B=68% C=28% 14 JPM, 1997
  • 16. Prospective study • Recruited 79 subjects • LT seroprevalence similar in HIV+ and HIV- • Overall prevalence of 64% 15
  • 17. Impact of LT on Brain 16
  • 19. 18
  • 22. • Case control study – 54 suicide attempters and 30 controls • Self-directed violence assessed by SUAS-S score J Clin Psy, Aug 2012 21
  • 23. • Violent suicide attempts, RR=1.81 (95% CI, 1.13-2.84) • Suicide, RR=2.05 (95% CI, 0.78-5.20) 22
  • 24. • First study to investigate the effect of LT in humans • Significant delay in reaction time in those with LT • Positive correlation between length of infection and mean reaction time 23
  • 25. 24
  • 26. • Prospective study of 3,890 male subjects • LT increased the chance of traffic accidents – (OR 2.43, CI95: 1.11–5.35, P = 0.027) • RhD positivity reduced the risk of traffic accidents in LT+ subjects – (OR 0.35, CI95: 0.136–0.902, P= 0.028) • RhD+ people are protected against LT-induced impaired reaction time 25
  • 27. • 758 women in 16th week of gestation • LT+ women had a lower body weight (p = 0.02) • Cumulative effect 26
  • 28. Other Effects of LTI • Alzheimer’s disease • Parkinson’s disease • Schizophrenia • OCD • Increases probability of birth of male offspring • Effect on personality – High intelligence, guilt proneness, radicalism, and high ergic tension 27
  • 29. 28
  • 30. Mechanism behind impact of LT on brain 29
  • 31. TH within cysts 30 PC12 cell culture
  • 32. • Cysts widely distributed in brain • Cerebral cortex had higher cyst density than subcortical region • Cerebellum consistently had low cysts • Myelinated fiber tracts devoid of cysts • No tropism towards dopaminergic or hypothalamic systems 31
  • 33. • Men with LT had decreased leukocyte, NK-cell and monocyte counts • Women had increased counts • B-cell counts were reduced in both men and women • The difference between LT+ and LT- subjects declined with decline in Toxo IgG titers 32
  • 35. Background • Prevalence of LT is similar or higher in HIV+ compared with HIV- individuals • ARVs do not affect LT • HIV-associated neurocognitive disorders persist despite adequate ART – Co-infections like LT may contribute to NCI • Impact of LT on neurocognitive impairment in HIV+ individuals has not been studied 34
  • 36. Objectives • To determine the prevalence of LT in our HIV+ cohort • To evaluate its impact on neurocognitive functioning 35
  • 37. Methods • Randomly selected 120 HIV+ participants from an NIH- funded cohort project • Toxoplasma IgG was measured in serum by commercial immunoassay • HNRC neurocognitive test battery was used – Tests 7 ability areas • Performance was summarized as the validated global deficit score (GDS) – GDS ≥ 0.5 defined neurocognitive impairment • Data were analyzed by routine statistical methods, including Pearson’s correlations and linear regression 36
  • 38. Neuropsychological Test Battery Verbal Fluency Executive Functioning Sound Category Test Animals WCST-64 Action Color Trails II Attn/Working Memory Learning/Memory PASAT-50 Verbal (Hopkins Verbal Learning WMS-III Spatial Span Test - Revised) Processing Speed Visual (Brief Visuospatial Memory Test - Revised) WAIS-III Digit Symbol WAIS-III Symbol Search Motor Trails A Grooved Pegboard Color Trails 1 37
  • 39. Results • LT was detected in 12 (10%) participants • LT+ subjects were similar to LT- subjects except that they were significantly older • LT+ subjects were more likely to have neurocognitive impairment (although not statistically significant) – This difference was greater among subjects who were older than the median age of 44 years (60% vs. 33%, p = 0.11) 38
  • 40. 39
  • 41. Results • LT was detected in 12 (10%) participants • LT+ subjects were similar to LT- subjects except that they were significantly older • LT+ subjects were more likely to have neurocognitive impairment (although not statistically significant) – This difference was greater among subjects who were older than the median age of 44 years (60% vs. 33%, p = 0.11) • Among LT+ subjects, higher IgG titers titers were associated with – higher CD4+ T-cell counts (r=0.74, p=0.05, Fig. 1) – worse GDS (r=0.31, p=0.33, Fig. 2) – On excluding the 2 outliers, worse GDS (r=0.88, p=0.0007, Fig. 2) – Higher memory deficit (p=0.01) 40
  • 42. Toxo titers and CD4+ count 41
  • 43. Results • LT was detected in 12 (10%) participants • LT+ subjects were similar to LT- subjects except that they were significantly older • LT+ subjects were more likely to have neurocognitive impairment (although not statistically significant) – This difference was greater among subjects who were older than the median age of 44 years (60% vs. 33%, p = 0.11) • Among LT+ subjects, higher IgG titers titers were associated with – higher CD4+ T-cell counts (r=0.74, p=0.05, Fig. 1) – worse GDS (r=0.31, p=0.33, Fig. 2) – On excluding the 2 outliers, worse GDS (r=0.88, p=0.0007, Fig. 2) – Higher memory deficit (p=0.01) 42
  • 44. Toxo Titers and GDS 43
  • 45. Results • LT was detected in 12 (10%) participants • LT+ subjects were similar to LT- subjects except that they were significantly older • LT+ subjects were more likely to have neurocognitive impairment (although not statistically significant) – This difference was greater among subjects who were older than the median age of 44 years (60% vs. 33%, p = 0.11) • Among LT+ subjects, higher IgG titers titers were associated with – higher CD4+ T-cell counts (r=0.74, p=0.05, Fig. 1) – worse GDS (r=0.31, p=0.33, Fig. 2) – On excluding the 2 outliers, worse GDS (r=0.88, p=0.0007, Fig. 2) – Higher memory deficit (p=0.01) 44
  • 46. Conclusions • Prevalence of LT in our HIV+ cohort was 10% – Similar to the general population (10.8%) – Not generalizable as our cohort consisted of drug abusers • LT+ older subjects trended towards worse neurocognitive functioning and higher anti-Toxo IgG titers were associated with worse functioning • Studies with a larger number of LT+ individuals are needed to validate this finding 45
  • 47. Future Directions • Identify a larger HIV and LT co-infected cohort – Owen clinic and HNRC • Investigate the impact on driving in more detail – Driving simulator studies • Mechanistic studies – Role of inflammation: plasma and CSF – In vitro brain model 46
  • 48. Malaria 47
  • 49. Malaria • Mosquito-borne infectious disease • Plasmodium spp. – P. falciparum, P. vivax – P. ovale, P. malariae • 300-500 million episodes of acute illness • > 1 million deaths/year worldwide 48
  • 51. Malaria and HIV Interactions • HIV+ patients are twice as likely to get malaria* • ↑HIV RNA and ↓CD4 counts • Malaria doubles HIV-1-RNA with 0.25 log ↑** • HIV RNA ↑ (0.82 log ↑) greatest when • Febrile patient • Parasite density >2,000/µL • CD4 >300/µL • Mathematical model • Village of ~200,000 had excess 8,500 HIV infections and 980,000 malaria episodes*** *Patnaik et al J Infect Dis 2005; **Kublin et al Lancet 2005; ***Kublin Science 2006 50
  • 52. 51
  • 53. Asymptomatic Malaria • Seen in areas of high transmission • Also reported in low edemicity regions • Clinical immunity that controls parasitemia but does not completely eliminate it • Described for both P. falciparum & P. vivax malaria • Few studies on HIV and asymptomatic malaria co- infections • Since malaria prevalence is not homogenous, sites need to be tested individually 52
  • 55. Study Objective • To retrospectively determine the prevalence of malaria co-infection in a cohort of HIV- infected individuals in southern India 54
  • 56. Methods • Individuals presenting to YRG CARE, Chennai, India between Jan 1, 2008 and Dec 31, 2008 • Stored serum samples randomly selected from HIV+ individuals • Retrospectively diagnosed malaria by antibody testing and PCR 55
  • 57. Results • Malaria co-infection rate 9.8% (45/460) • PCR negative 56
  • 58. Discussion • Considerable burden of malaria co-infection • Predominently due to P. vivax • Rate of P. falciparum 6-fold higher than in the general population • Co-infected subjects not more likely to be immunosupressed than HIV mono-infected • Negative PCR – Possibly due to parasitemia below detection limit – Parasite DNA degradation unlikely • Our strategy may be used for identifying co- infections in areas with unstable malaria transmission 57
  • 59. Future Directions • Alternate site with high malaria prevalence – Nigeria • Use of more suitable specimens – Whole blood or Dried blood spots 58
  • 60. 59
  • 61. Acknowledgements • United States • India – Scott Letendre – N. Kumarasamy – Davey Smith – Jabin – Tom Marcotte – Ron Ellis • Nigeria – Connie Benson – Kanayo Okwuasaba – Chip Schooley – Ndidi Agala – Igor Grant – Allen McCutchan • Funding – Cris Achim – NIMH 1 K23 MH085512-01A2 – D. J. Perkins – CFAR International Pilot Project Grant – Walter Royal • Study participants 60